A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752291



Internal ID12985843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26265536..26395885hg38UCSC Ensembl
Innerchr9:26265534..26395883hg19UCSC Ensembl
Innerchr9:26255534..26385883hg18UCSC Ensembl
Innerchr9:26255534..26385883hg17UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38130350
hg19130350
hg18130350
hg17130350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6983945, essv6983946
SamplesBEC_736
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)esv2752291
Frequency
Sample Size771
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer