A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619973



Internal ID7006846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21950536..21952665hg38UCSC Ensembl
Innerchr9:21950566..21952636hg38UCSC Ensembl
Outerchr9:21950507..21952695hg38UCSC Ensembl
chr9:21950535..21952664hg19UCSC Ensembl
Innerchr9:21950565..21952635hg19UCSC Ensembl
Outerchr9:21950506..21952694hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg382130
hg192130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13420806, essv13420807
SamplesHG01164, HG01670
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619973
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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