A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979917



Internal ID12980931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:629468..689340hg38UCSC Ensembl
Innerchr9:629468..689340hg19UCSC Ensembl
Innerchr9:619468..679340hg18UCSC Ensembl
Innerchr9:619468..679340hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3859873
hg1959873
hg1859873
hg1759873
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 Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6979917
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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