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dbVar

Database of genomic structural variation

nsv437051

Organism: Homo sapiens

Study:nstd17 (Conrad et al. 2005)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:NCBI34 (hg16)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:67,215

Publication(s):Conrad et al. 2005

Links to Other Resources

Overlapping Genes

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: 519 SVs from 62 studies. See in: genome view

Remapped(Score: Perfect):14,915,678-14,982,892

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
nsv437051	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	14,915,678	14,926,227	14,974,778	14,982,892
nsv437051	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	14,773,187	14,783,736	14,832,287	14,840,401
nsv437051	Submitted genomic		NCBI34 (hg16)	Primary Assembly		NC_000008.8	Chr8	14,783,553	14,794,102	14,842,653	14,850,767

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv466932	copy number loss	NA10863	SNP array	SNP genotyping analysis	Heterozygous	20

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv466932	Remapped	Perfect	NC_000008.11:g.(14 915678_14926227)_( 14974778_14982892) del	GRCh38.p12	First Pass	NC_000008.11	Chr8	14,915,678	14,926,227	14,974,778	14,982,892
nssv466932	Remapped	Perfect	NC_000008.10:g.(14 773187_14783736)_( 14832287_14840401) del	GRCh37.p13	First Pass	NC_000008.10	Chr8	14,773,187	14,783,736	14,832,287	14,840,401
nssv466932	Submitted genomic		NC_000008.8:g.(147 83553_14794102)_(1 4842653_14850767)d el	NCBI34 (hg16)		NC_000008.8	Chr8	14,783,553	14,794,102	14,842,653	14,850,767

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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