A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063312



Internal ID18805843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:33567686..33587987hg38UCSC Ensembl
Innerchr22:33963672..33983973hg19UCSC Ensembl
Innerchr22:32293672..32313973hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3820302
hg1920302
hg1820302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3734204
Samples
Known GenesLARGE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063312
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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