A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6982857



Internal ID12975655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1062220..1823899hg38UCSC Ensembl
Innerchr9:1062220..1823899hg19UCSC Ensembl
Innerchr9:1052220..1813899hg18UCSC Ensembl
Innerchr9:1052220..1813899hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38761680
hg19761680
hg18761680
hg17761680
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752273
Supporting Variants
SamplesBEC_605
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6982857
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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