A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984362



Internal ID12976866
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 StatusS
Merged Variantsesv2752132
Supporting Variants
SamplesBEC_694
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984362
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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