A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv674866



Internal ID15411518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70651742..70884757hg38UCSC Ensembl
InnerchrX:69871592..70104607hg19UCSC Ensembl
InnerchrX:69788317..70021332hg18UCSC Ensembl
InnerchrX:69654613..69887628hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg38233016
hg19233016
hg18233016
hg17233016
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv674866
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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