A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616203



Internal ID7003090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9851105..9851500hg38UCSC Ensembl
Innerchr8:9851124..9851482hg38UCSC Ensembl
Outerchr8:9851087..9851519hg38UCSC Ensembl
chr8:9708615..9709010hg19UCSC Ensembl
Innerchr8:9708634..9708992hg19UCSC Ensembl
Outerchr8:9708597..9709029hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38396
hg19396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13099233, essv13099234
SamplesHG01812, HG02137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616203
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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