A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695782



Internal ID15432434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:88230705..88336642hg38UCSC Ensembl
InnerchrX:87485706..87591643hg19UCSC Ensembl
InnerchrX:87372362..87478299hg18UCSC Ensembl
InnerchrX:87291851..87397788hg17UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg38105938
hg19105938
hg18105938
hg17105938
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518355
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695782
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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