A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666507



Internal ID15403159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:35989497..36160511hg38UCSC Ensembl
InnerchrX:36007614..36178628hg19UCSC Ensembl
InnerchrX:35917535..36088549hg18UCSC Ensembl
InnerchrX:35767271..35938285hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38171015
hg19171015
hg18171015
hg17171015
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516150
Supporting Variants
Samples
Known GenesCHDC2, CXorf22, LOC101928564
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666507
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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