nsv932782
- Organism: Homo sapiens
- Study:nstd79 (Dittwald et al. 2013)
- Variant Type:copy number variation
- Method Type:Oligo aCGH
- Submitted on:GRCh37 (hg19)
- Variant Calls:9
- Validation:Not tested
- Clinical Assertions: No
- Region Size:94,061
- Publication(s):Dittwald et al. 2013
Source: NCBI
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 517 SVs from 72 studies. See in: genome view
Overlapping variant regions from other studies: 517 SVs from 72 studies. See in: genome view
Variant Region Placement Information
Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nsv932782 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000010.11 | Chr10 | 14,932,845 | 14,944,568 | 15,015,361 | 15,026,905 |
nsv932782 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000010.10 | Chr10 | 14,974,844 | 14,986,567 | 15,057,360 | 15,068,904 |
Variant Call Information
Variant Call ID | Type | Sample ID | Method | Analysis |
---|---|---|---|---|
nssv1610663 | deletion | 1015 | Oligo aCGH | Probe signal intensity |
nssv1610732 | deletion | 826 | Oligo aCGH | Probe signal intensity |
nssv1611284 | deletion | 1261 | Oligo aCGH | Probe signal intensity |
nssv1611320 | deletion | 885 | Oligo aCGH | Probe signal intensity |
nssv1611687 | deletion | 699 | Oligo aCGH | Probe signal intensity |
nssv1612424 | deletion | 799 | Oligo aCGH | Probe signal intensity |
nssv1612821 | deletion | 1264 | Oligo aCGH | Probe signal intensity |
nssv1611796 | deletion | 695 | Oligo aCGH | Probe signal intensity |
nssv1611684 | deletion | 560 | Oligo aCGH | Probe signal intensity |
Variant Call Placement Information
Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Inner Start | Inner Stop | Outer Stop |
---|---|---|---|---|---|---|---|---|---|---|---|
nssv1610663 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1610732 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1611284 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1611320 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1611687 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1612424 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1612821 | Remapped | Perfect | NC_000010.11:g.(14 932839_14944974)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,932,839 | 14,944,974 | 14,973,283 | 15,043,963 |
nssv1611796 | Remapped | Perfect | NC_000010.11:g.(14 935697_14936201)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,935,697 | 14,936,201 | 14,973,283 | 15,043,963 |
nssv1611684 | Remapped | Perfect | NC_000010.11:g.(14 936756_14939606)_( 14973283_15043963) del | GRCh38.p12 | First Pass | NC_000010.11 | Chr10 | 14,936,756 | 14,939,606 | 14,973,283 | 15,043,963 |
nssv1610663 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1610732 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1611284 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1611320 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1611687 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1612424 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1612821 | Remapped | Perfect | NC_000010.10:g.(14 974838_14986973)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,974,838 | 14,986,973 | 15,015,282 | 15,085,962 |
nssv1611796 | Remapped | Perfect | NC_000010.10:g.(14 977696_14978200)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,977,696 | 14,978,200 | 15,015,282 | 15,085,962 |
nssv1611684 | Remapped | Perfect | NC_000010.10:g.(14 978755_14981605)_( 15015282_15085962) del | GRCh37.p13 | First Pass | NC_000010.10 | Chr10 | 14,978,755 | 14,981,605 | 15,015,282 | 15,085,962 |
nssv1610663 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1610732 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1611284 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1611320 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1611687 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1612424 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1612821 | Submitted genomic | NC_000010.9:g.(150 14844_15026979)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,014,844 | 15,026,979 | 15,055,288 | 15,125,968 | ||
nssv1611796 | Submitted genomic | NC_000010.9:g.(150 17702_15018206)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,017,702 | 15,018,206 | 15,055,288 | 15,125,968 | ||
nssv1611684 | Submitted genomic | NC_000010.9:g.(150 18761_15021611)_(1 5055288_15125968)d el | NCBI36 (hg18) | NC_000010.9 | Chr10 | 15,018,761 | 15,021,611 | 15,055,288 | 15,125,968 |