A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987772



Internal ID12978261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7296644..7779772hg38UCSC Ensembl
Innerchr9:7296644..7779772hg19UCSC Ensembl
Innerchr9:7286644..7769772hg18UCSC Ensembl
Innerchr9:7286644..7769772hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38483129
hg19483129
hg18483129
hg17483129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34566
Supporting Variants
SamplesNA07345
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987772
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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