A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979921



Internal ID12980967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:612167..718872hg38UCSC Ensembl
Innerchr9:612167..718872hg19UCSC Ensembl
Innerchr9:602167..708872hg18UCSC Ensembl
Innerchr9:602167..708872hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38106706
hg19106706
hg18106706
hg17106706
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34685
Supporting Variants
SamplesNA18860
Known GenesKANK1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979921
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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