U.S. flag

An official website of the United States government

nsv5485094

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,960

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
Submitted genomic98,084,146-98,087,105Question Mark
Overlapping variant regions from other studies: 118 SVs from 23 studies. See in: genome view    
Remapped(Score: Perfect):100,846,428-100,849,387Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5485094Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000009.12Chr998,084,14698,087,105
nsv5485094RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr9100,846,428100,849,387

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17026873deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17026873Submitted genomicNC_000009.12:g.980
84146_98087105del
GRCh38 (hg38)NC_000009.12Chr998,084,14698,087,105
nssv17026873RemappedPerfectNC_000009.11:g.100
846428_100849387de
l
GRCh37.p13First PassNC_000009.11Chr9100,846,428100,849,387

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv17026873<0.00166404
Support Center