A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980112



Internal ID12981282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:62766866..62986466hg38UCSC Ensembl
Innerchr13:63340999..63560599hg19UCSC Ensembl
Innerchr13:62239000..62458600hg18UCSC Ensembl
Innerchr13:62239000..62458600hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38219601
hg19219601
hg18219601
hg17219601
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)essv6980112
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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