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nsv4542335

  • 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: 48 SVs from 10 studies. See in: genome view    
Remapped(Score: Perfect):129,979,452-129,979,452Question Mark
Overlapping variant regions from other studies: 48 SVs from 10 studies. See in: genome view    
Submitted genomic130,737,025-130,737,025Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4542335RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000002.12Chr2129,979,452129,979,452
nsv4542335Submitted genomicGRCh37.p13Primary AssemblyNC_000002.11Chr2130,737,025130,737,025

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16040215insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16040215RemappedPerfectNC_000002.12:g.129
979452_129979453in
s186
GRCh38.p12First PassNC_000002.12Chr2129,979,452129,979,452
nssv16040215Submitted genomicNC_000002.11:g.130
737025_130737026in
s186
GRCh37.p13NC_000002.11Chr2130,737,025130,737,025

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)
nssv16040215<0.001321690
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