A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979922



Internal ID12980956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:629468..678088hg38UCSC Ensembl
Innerchr9:629468..678088hg19UCSC Ensembl
Innerchr9:619468..668088hg18UCSC Ensembl
Innerchr9:619468..668088hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3848621
hg1948621
hg1848621
hg1748621
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)essv6979922
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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