A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981531



Internal ID12972263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11224627..11562051hg38UCSC Ensembl
Innerchr9:11224627..11562051hg19UCSC Ensembl
Innerchr9:11214627..11552051hg18UCSC Ensembl
Innerchr9:11214627..11552051hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38337425
hg19337425
hg18337425
hg17337425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752275
Supporting Variants
SamplesBEC_293
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981531
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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