A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699124



Internal ID15435776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112421779..112543556hg38UCSC Ensembl
InnerchrX:111665007..111786784hg19UCSC Ensembl
InnerchrX:111551663..111673440hg18UCSC Ensembl
InnerchrX:111471152..111592929hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38121778
hg19121778
hg18121778
hg17121778
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523375
Supporting Variants
Samples
Known GenesZCCHC16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699124
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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