A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979722



Internal ID12633948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35060310..35164393hg38UCSC Ensembl
Innerchr22:35456303..35560386hg19UCSC Ensembl
Innerchr22:33786303..33890386hg18UCSC Ensembl
Innerchr22:33780857..33884940hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38104084
hg19104084
hg18104084
hg17104084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35003
Supporting Variants
SamplesNA18612
Known GenesISX
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979722
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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