A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620314



Internal ID7007185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33010864..33012340hg38UCSC Ensembl
Innerchr9:33010901..33012303hg38UCSC Ensembl
Outerchr9:33010827..33012377hg38UCSC Ensembl
chr9:33010862..33012338hg19UCSC Ensembl
Innerchr9:33010899..33012301hg19UCSC Ensembl
Outerchr9:33010825..33012375hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg381477
hg191477
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13451451
SamplesHG03908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620314
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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