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nsv4972821

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,938

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 138 SVs from 46 studies. See in: genome view    
Submitted genomic55,310,668-55,331,605Question Mark
Overlapping variant regions from other studies: 138 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):55,704,452-55,725,389Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4972821Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1255,310,66855,331,605
nsv4972821RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1255,704,45255,725,389

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16537252deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16537252Submitted genomicNC_000012.12:g.553
10668_55331605del
GRCh38 (hg38)NC_000012.12Chr1255,310,66855,331,605
nssv16537252RemappedPerfectNC_000012.11:g.557
04452_55725389del
GRCh37.p13First PassNC_000012.11Chr1255,704,45255,725,389

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16537252<0.001129246
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