A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752278



Internal ID12985830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11600500..11701727hg38UCSC Ensembl
Innerchr9:11600500..11701727hg19UCSC Ensembl
Innerchr9:11590500..11691727hg18UCSC Ensembl
Innerchr9:11590500..11691727hg17UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38101228
hg19101228
hg18101228
hg17101228
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6982682, essv6982683
SamplesBEC_579
Known Genes
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)esv2752278
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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