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nsv5563814

  • 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: 68 SVs from 14 studies. See in: genome view    
Submitted genomic93,250,689-93,250,740Question Mark
Overlapping variant regions from other studies: 70 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):93,717,035-93,717,086Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563814Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1493,250,68993,250,740
nsv5563814RemappedPerfectGRCh37.p13Primary AssemblySecond PassNC_000014.8Chr1493,717,03593,717,086

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699509sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699509Submitted genomicNC_000014.9:g.9325
0689_93250740ins13
14
GRCh38 (hg38)NC_000014.9Chr1493,250,68993,250,740
nssv17699509RemappedPerfectNC_000014.8:g.9371
7035_93717086ins13
14
GRCh37.p13Second PassNC_000014.8Chr1493,717,03593,717,086

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)
nssv17699509<0.00136404
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