A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676513



Internal ID15413165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:5684069..5721710hg38UCSC Ensembl
InnerchrX:5602110..5639751hg19UCSC Ensembl
InnerchrX:5612110..5649751hg18UCSC Ensembl
InnerchrX:5461846..5499487hg17UCSC Ensembl
CytobandXp22.32
Allele length
AssemblyAllele length
hg3837642
hg1937642
hg1837642
hg1737642
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515922
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676513
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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