A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984873



Internal ID12983636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102077163..102180163hg38UCSC Ensembl
Innerchr9:104839445..104942445hg19UCSC Ensembl
Innerchr9:103879266..103982266hg18UCSC Ensembl
Innerchr9:101919000..102022000hg17UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38103001
hg19103001
hg18103001
hg17103001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752272
Supporting Variants
SamplesSPC_188
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984873
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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