U.S. flag

An official website of the United States government

nsv4577700

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Remapped(Score: Perfect):25,041,672-25,041,672Question Mark
Overlapping variant regions from other studies: 18 SVs from 4 studies. See in: genome view    
Submitted genomic25,330,601-25,330,601Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4577700RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000010.11Chr1025,041,67225,041,672
nsv4577700Submitted genomicGRCh37.p13Primary AssemblyNC_000010.10Chr1025,330,60125,330,601

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15992076sva insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15992076RemappedPerfectNC_000010.11:g.250
41672_25041673ins1
240
GRCh38.p12First PassNC_000010.11Chr1025,041,67225,041,672
nssv15992076Submitted genomicNC_000010.10:g.253
30601_25330602ins1
240
GRCh37.p13NC_000010.10Chr1025,330,60125,330,601

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)
nssv15992076<0.001321692
Support Center