A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664700



Internal ID15401352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96991046..97148121hg38UCSC Ensembl
InnerchrX:96246045..96403120hg19UCSC Ensembl
InnerchrX:96132701..96289776hg18UCSC Ensembl
InnerchrX:96052190..96209265hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38157076
hg19157076
hg18157076
hg17157076
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)nssv664700
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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