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nsv5504673

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,480

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 91 SVs from 32 studies. See in: genome view    
Submitted genomic46,822,342-46,825,821Question Mark
Overlapping variant regions from other studies: 91 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):47,216,125-47,219,604Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5504673Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1246,822,34246,825,821
nsv5504673RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1247,216,12547,219,604

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17056758duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17056758Submitted genomicNC_000012.12:g.468
22342_46825821dup
GRCh38 (hg38)NC_000012.12Chr1246,822,34246,825,821
nssv17056758RemappedPerfectNC_000012.11:g.472
16125_47219604dup
GRCh37.p13First PassNC_000012.11Chr1247,216,12547,219,604

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)
nssv17056758<0.00116404
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