A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6989932



Internal ID12977895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:83526795..83708519hg38UCSC Ensembl
Innerchr13:84100930..84282654hg19UCSC Ensembl
Innerchr13:82998931..83180655hg18UCSC Ensembl
Innerchr13:82998931..83180655hg17UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38181725
hg19181725
hg18181725
hg17181725
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2751153
Supporting Variants
SamplesBEC_814
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6989932
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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