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nsv5511656

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:113

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
Submitted genomic47,852,599-47,852,711Question Mark
Overlapping variant regions from other studies: 84 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):48,246,382-48,246,494Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5511656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1247,852,59947,852,711
nsv5511656RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1248,246,38248,246,494

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056848duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056848Submitted genomicNC_000012.12:g.478
52599_47852711dup
GRCh38 (hg38)NC_000012.12Chr1247,852,59947,852,711
nssv17056848RemappedPerfectNC_000012.11:g.482
46382_48246494dup
GRCh37.p13First PassNC_000012.11Chr1248,246,38248,246,494

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)
nssv17056848<0.00116404
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