A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752132



Internal ID12985684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:9264658..9328286hg38UCSC Ensembl
Innerchr6:9264891..9328519hg19UCSC Ensembl
Innerchr6:9372877..9436505hg18UCSC Ensembl
Innerchr6:9372877..9436505hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3863629
hg1963629
hg1863629
hg1763629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6984363, essv6984362
SamplesBEC_694
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752132
Frequency
Sample Size771
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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