U.S. flag

An official website of the United States government

nsv5550255

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 114 SVs from 28 studies. See in: genome view    
Submitted genomic118,041,927-118,041,978Question Mark
Overlapping variant regions from other studies: 114 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):118,963,082-118,963,133Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5550255Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000004.12Chr4118,041,927118,041,978
nsv5550255RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000004.11Chr4118,963,082118,963,133

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16954039insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16954039Submitted genomicNC_000004.12:g.118
041927_118041978in
s321
GRCh38 (hg38)NC_000004.12Chr4118,041,927118,041,978
nssv16954039RemappedPerfectNC_000004.11:g.118
963082_118963133in
s321
GRCh37.p13First PassNC_000004.11Chr4118,963,082118,963,133

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)
nssv16954039<0.00116404
Support Center