A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6983981



Internal ID12977491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:65314081..65468489hg38UCSC Ensembl
Innerchr13:65888213..66042621hg19UCSC Ensembl
Innerchr13:64786214..64940622hg18UCSC Ensembl
Innerchr13:64786214..64940622hg17UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38154409
hg19154409
hg18154409
hg17154409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751147
Supporting Variants
SamplesBEC_74
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6983981
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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