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nsv5563437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:53

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 134 SVs from 32 studies. See in: genome view    
Submitted genomic24,061,224-24,061,276Question Mark
Overlapping variant regions from other studies: 134 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):24,244,026-24,244,078Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1924,061,22424,061,276
nsv5563437RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1924,244,02624,244,078

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722563line1 insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722563Submitted genomicNC_000019.10:g.240
61224_24061276ins6
014
GRCh38 (hg38)NC_000019.10Chr1924,061,22424,061,276
nssv17722563RemappedPerfectNC_000019.9:g.2424
4026_24244078ins60
14
GRCh37.p13First PassNC_000019.9Chr1924,244,02624,244,078

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)
nssv17722563<0.00136402
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