A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6988267



Internal ID12980954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:635500..699065hg38UCSC Ensembl
Innerchr9:635500..699065hg19UCSC Ensembl
Innerchr9:625500..689065hg18UCSC Ensembl
Innerchr9:625500..689065hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3863566
hg1963566
hg1863566
hg1763566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35002
Supporting Variants
SamplesNA18859
Known GenesKANK1
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6988267
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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