U.S. flag

An official website of the United States government

nsv4207706

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:295,644

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 251 SVs from 17 studies. See in: genome view    
Remapped(Score: Perfect):58,716,104-59,011,747Question Mark
Overlapping variant regions from other studies: 251 SVs from 17 studies. See in: genome view    
Submitted genomic58,483,577-58,779,220Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4207706RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000011.10Chr1158,716,10459,011,747
nsv4207706Submitted genomicGRCh37.p13Primary AssemblyNC_000011.9Chr1158,483,57758,779,220

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15950432duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15950432RemappedPerfectNC_000011.10:g.587
16104_59011747dup
GRCh38.p12First PassNC_000011.10Chr1158,716,10459,011,747
nssv15950432Submitted genomicNC_000011.9:g.5848
3577_58779220dup
GRCh37.p13NC_000011.9Chr1158,483,57758,779,220

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)
nssv159504324.6e-005121694
Support Center