A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980662



Internal ID12971767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11224627..11958106hg38UCSC Ensembl
Innerchr9:11224627..11958106hg19UCSC Ensembl
Innerchr9:11214627..11948106hg18UCSC Ensembl
Innerchr9:11214627..11948106hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38733480
hg19733480
hg18733480
hg17733480
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752276
Supporting Variants
SamplesBEC_101
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980662
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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