A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6979916



Internal ID12980932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:613260..689340hg38UCSC Ensembl
Innerchr9:613260..689340hg19UCSC Ensembl
Innerchr9:603260..679340hg18UCSC Ensembl
Innerchr9:603260..679340hg17UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg3876081
hg1976081
hg1876081
hg1776081
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)essv6979916
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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