A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661775



Internal ID15398427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70720583..70819919hg38UCSC Ensembl
InnerchrX:69940433..70039769hg19UCSC Ensembl
InnerchrX:69857158..69956494hg18UCSC Ensembl
InnerchrX:69723454..69822790hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3899337
hg1999337
hg1899337
hg1799337
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)nssv661775
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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