A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv711294



Internal ID16005250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22060729..22064204hg38UCSC Ensembl
Innerchr1:22387222..22390697hg19UCSC Ensembl
Innerchr1:22259809..22263284hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383476
hg193476
hg183476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv545746
Supporting Variants
Samples
Known GenesCDC42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv711294
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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