A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617872



Internal ID7004756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85055761..85063498hg38UCSC Ensembl
Innerchr8:85055763..85063496hg38UCSC Ensembl
Outerchr8:85055759..85063500hg38UCSC Ensembl
chr8:85967996..85975733hg19UCSC Ensembl
Innerchr8:85967998..85975731hg19UCSC Ensembl
Outerchr8:85967994..85975735hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg387738
hg197738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13246011, essv13246012, essv13246010
SamplesHG03548, HG03077, HG03439
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617872
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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