A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663456



Internal ID15400108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:97017139..97148876hg38UCSC Ensembl
InnerchrX:96272138..96403875hg19UCSC Ensembl
InnerchrX:96158794..96290531hg18UCSC Ensembl
InnerchrX:96078283..96210020hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38131738
hg19131738
hg18131738
hg17131738
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515760
Supporting Variants
Samples
Known GenesDIAPH2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663456
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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