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nsv62

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52,319

Genome View

Select assembly:
Overlapping variant regions from other studies: 603 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):1,908,931-1,961,249Question Mark
Overlapping variant regions from other studies: 603 SVs from 78 studies. See in: genome view    
Remapped(Score: Perfect):1,930,161-1,982,479Question Mark
Overlapping variant regions from other studies: 19 SVs from 8 studies. See in: genome view    
Submitted genomic1,886,737-1,939,055Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv62RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr111,908,9311,961,249
nsv62RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr111,930,1611,982,479
nsv62Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000011.8Chr111,886,7371,939,055

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv62inversionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv62RemappedPerfectNC_000011.10:g.(19
08931_?)_(?_196124
9)inv
GRCh38.p12First PassNC_000011.10Chr111,908,9311,961,249
nssv62RemappedPerfectNC_000011.9:g.(193
0161_?)_(?_1982479
)inv
GRCh37.p13First PassNC_000011.9Chr111,930,1611,982,479
nssv62Submitted genomicNC_000011.8:g.(188
6737_?)_(?_1939055
)inv
NCBI35 (hg17)NC_000011.8Chr111,886,7371,939,055

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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