A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984778



Internal ID12636818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20262761..20383361hg38UCSC Ensembl
Innerchr13:20836900..20957500hg19UCSC Ensembl
Innerchr13:19734900..19855500hg18UCSC Ensembl
Innerchr13:19734900..19855500hg17UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38120601
hg19120601
hg18120601
hg17120601
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751132
Supporting Variants
SamplesSPC_179
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984778
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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