A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978162



Internal ID12981520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62766885..63028790hg38UCSC Ensembl
Innerchr13:63341018..63602923hg19UCSC Ensembl
Innerchr13:62239019..62500924hg18UCSC Ensembl
Innerchr13:62239019..62500924hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38261906
hg19261906
hg18261906
hg17261906
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)essv6978162
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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