A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984405



Internal ID12630251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6704475..6908195hg38UCSC Ensembl
Innerchr9:6704475..6908195hg19UCSC Ensembl
Innerchr9:6694475..6898195hg18UCSC Ensembl
Innerchr9:6694475..6898195hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38203721
hg19203721
hg18203721
hg17203721
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752309
Supporting Variants
SamplesBEC_703
Known GenesKDM4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984405
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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