A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656818



Internal ID15393470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:20796312..21018764hg38UCSC Ensembl
InnerchrX:20814430..21036882hg19UCSC Ensembl
InnerchrX:20724351..20946803hg18UCSC Ensembl
InnerchrX:20574087..20796539hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg38222453
hg19222453
hg18222453
hg17222453
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517746
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656818
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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