U.S. flag

An official website of the United States government

nsv5498590

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:26,241,002

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 87856 SVs from 141 studies. See in: genome view    
Submitted genomic80,522,636-106,763,637Question Mark
Overlapping variant regions from other studies: 84111 SVs from 141 studies. See in: genome view    
Remapped(Score: Good):80,988,980-106,929,356Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5498590Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1480,522,636106,763,637
nsv5498590RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1480,988,980106,929,356

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17698994duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17698994Submitted genomicNC_000014.9:g.8052
2636_106763637dup
GRCh38 (hg38)NC_000014.9Chr1480,522,636106,763,637
nssv17698994RemappedGoodNC_000014.8:g.8098
8980_106929356dup
GRCh37.p13First PassNC_000014.8Chr1480,988,980106,929,356

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)
nssv17698994<0.00126402
Support Center