A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619616



Internal ID6659802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:11600555..11733459hg38UCSC Ensembl
Innerchr9:11600596..11733418hg38UCSC Ensembl
Outerchr9:11600514..11733500hg38UCSC Ensembl
chr9:11600555..11733459hg19UCSC Ensembl
Innerchr9:11600596..11733418hg19UCSC Ensembl
Outerchr9:11600514..11733500hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38132905
hg19132905
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13403548, essv13403549
SamplesHG03028, HG00123
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619616
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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