A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989890



Internal ID12977481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:86038764..86112364hg38UCSC Ensembl
Innerchr13:86612899..86686499hg19UCSC Ensembl
Innerchr13:85510900..85584500hg18UCSC Ensembl
Innerchr13:85510900..85584500hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3873601
hg1973601
hg1873601
hg1773601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751155
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)essv6989890
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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