A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752309



Internal ID12639175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6670448..6908200hg38UCSC Ensembl
Innerchr9:6670448..6908200hg19UCSC Ensembl
Innerchr9:6660448..6898200hg18UCSC Ensembl
Innerchr9:6660448..6898200hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38237753
hg19237753
hg18237753
hg17237753
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6984405, essv6984404, essv6988800, essv6987590
SamplesBEC_703
Known GenesKDM4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752309
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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