A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv666686



Internal ID15056652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152894702..152963989hg38UCSC Ensembl
InnerchrX:152063246..152132533hg19UCSC Ensembl
InnerchrX:151813902..151883189hg18UCSC Ensembl
InnerchrX:151733814..151803101hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3869288
hg1969288
hg1869288
hg1769288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517284
Supporting Variants
Samples
Known GenesZNF185
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv666686
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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