A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978161



Internal ID12981538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62766866..62917266hg38UCSC Ensembl
Innerchr13:63340999..63491399hg19UCSC Ensembl
Innerchr13:62239000..62389400hg18UCSC Ensembl
Innerchr13:62239000..62389400hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38150401
hg19150401
hg18150401
hg17150401
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34669
Supporting Variants
SamplesNA18973
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978161
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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