A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6978537



Internal ID12978712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:1206411..1382861hg38UCSC Ensembl
Innerchr9:1206411..1382861hg19UCSC Ensembl
Innerchr9:1196411..1372861hg18UCSC Ensembl
Innerchr9:1196411..1372861hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38176451
hg19176451
hg18176451
hg17176451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34351
Supporting Variants
SamplesNA11882
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6978537
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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