A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6980563



Internal ID12635929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:112621165..112804165hg38UCSC Ensembl
Innerchr9:115383445..115566445hg19UCSC Ensembl
Innerchr9:114423266..114606266hg18UCSC Ensembl
Innerchr9:112463000..112646000hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38183001
hg19183001
hg18183001
hg17183001
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv34763
Supporting Variants
SamplesNA19209
Known GenesINIP, KIAA1958, SNX30
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6980563
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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