A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980111



Internal ID12981281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62707806..63063144hg38UCSC Ensembl
Innerchr13:63281939..63637277hg19UCSC Ensembl
Innerchr13:62179940..62535278hg18UCSC Ensembl
Innerchr13:62179940..62535278hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38355339
hg19355339
hg18355339
hg17355339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34296
Supporting Variants
SamplesNA18956
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980111
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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