A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981464



Internal ID12625464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:242362843..242730382hg17UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg17367540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751859
Supporting Variants
SamplesBEC_236
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981464
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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