A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979923



Internal ID12980968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:629468..705168hg38UCSC Ensembl
Innerchr9:629468..705168hg19UCSC Ensembl
Innerchr9:619468..695168hg18UCSC Ensembl
Innerchr9:619468..695168hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3875701
hg1975701
hg1875701
hg1775701
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)essv6979923
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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