U.S. flag

An official website of the United States government

nsv4189549

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:5,574

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 105 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):34,645,665-34,651,238Question Mark
Overlapping variant regions from other studies: 106 SVs from 7 studies. See in: genome view    
Submitted genomic34,645,662-34,651,235Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4189549RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr934,645,66534,651,238
nsv4189549Submitted genomicGRCh37.p13Primary AssemblyNC_000009.11Chr934,645,66234,651,235

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15935794deletionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15935794RemappedPerfectNC_000009.12:g.346
45665_34651238del
GRCh38.p12First PassNC_000009.12Chr934,645,66534,651,238
nssv15935794Submitted genomicNC_000009.11:g.346
45662_34651235del
GRCh37.p13NC_000009.11Chr934,645,66234,651,235

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)
nssv15935794<0.001421694
Support Center