A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752298



Internal ID12985850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30361740..30661614hg38UCSC Ensembl
Innerchr9:30361738..30661612hg19UCSC Ensembl
Innerchr9:30351738..30651612hg18UCSC Ensembl
Innerchr9:30351738..30651612hg17UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38299875
hg19299875
hg18299875
hg17299875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6984187, essv6989928, essv6984188
SamplesBEC_799
Known GenesLOC401497
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752298
Frequency
Sample Size771
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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