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nsv5424071

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:81,164

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 538 SVs from 65 studies. See in: genome view    
Submitted genomic9,270,732-9,351,895Question Mark
Overlapping variant regions from other studies: 538 SVs from 65 studies. See in: genome view    
Remapped(Score: Perfect):9,330,791-9,411,954Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5424071Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr19,270,7329,351,895
nsv5424071RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr19,330,7919,411,954

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16890222duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16890222Submitted genomicNC_000001.11:g.927
0732_9351895dup
GRCh38 (hg38)NC_000001.11Chr19,270,7329,351,895
nssv16890222RemappedPerfectNC_000001.10:g.933
0791_9411954dup
GRCh37.p13First PassNC_000001.10Chr19,330,7919,411,954

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)
nssv16890222<0.00116404
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