A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980816



Internal ID12982115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:12296100..12572100hg38UCSC Ensembl
Innerchr9:12296100..12572100hg19UCSC Ensembl
Innerchr9:12286100..12562100hg18UCSC Ensembl
Innerchr9:12286100..12562100hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38276001
hg19276001
hg18276001
hg17276001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34901
Supporting Variants
SamplesNA19130
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980816
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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