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nsv5527012

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:378

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 164 SVs from 20 studies. See in: genome view    
Submitted genomic28,176,253-28,176,630Question Mark
Overlapping variant regions from other studies: 164 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):25,756,217-25,756,594Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5527012Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000018.10Chr1828,176,25328,176,630
nsv5527012RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000018.9Chr1825,756,21725,756,594

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17716875deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17716875Submitted genomicNC_000018.10:g.281
76253_28176630del
GRCh38 (hg38)NC_000018.10Chr1828,176,25328,176,630
nssv17716875RemappedPerfectNC_000018.9:g.2575
6217_25756594del
GRCh37.p13First PassNC_000018.9Chr1825,756,21725,756,594

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)
nssv17716875<0.00126404
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