A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619824



Internal ID7006698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:16890592..16894505hg38UCSC Ensembl
Innerchr9:16890609..16894489hg38UCSC Ensembl
Outerchr9:16890576..16894522hg38UCSC Ensembl
chr9:16890590..16894503hg19UCSC Ensembl
Innerchr9:16890607..16894487hg19UCSC Ensembl
Outerchr9:16890574..16894520hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg383914
hg193914
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13411491, essv13411490
SamplesNA19384, HG03124
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619824
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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