A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600782



Internal ID18552377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25507736..25642811hg38UCSC Ensembl
Innerchr22:25903703..26038778hg19UCSC Ensembl
Innerchr22:24233703..24368778hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38135076
hg19135076
hg18135076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058343
Supporting Variants
Samples
Known GenesADRBK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600782
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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