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nsv5505576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,023

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 109 SVs from 28 studies. See in: genome view    
Submitted genomic55,785,342-55,787,364Question Mark
Overlapping variant regions from other studies: 109 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):56,179,126-56,181,148Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5505576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1255,785,34255,787,364
nsv5505576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,179,12656,181,148

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17057776deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17057776Submitted genomicNC_000012.12:g.557
85342_55787364del
GRCh38 (hg38)NC_000012.12Chr1255,785,34255,787,364
nssv17057776RemappedPerfectNC_000012.11:g.561
79126_56181148del
GRCh37.p13First PassNC_000012.11Chr1256,179,12656,181,148

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)
nssv17057776<0.00116404
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