A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617886



Internal ID7004770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:85602471..85651257hg38UCSC Ensembl
Innerchr8:85602486..85651243hg38UCSC Ensembl
Outerchr8:85602457..85651272hg38UCSC Ensembl
chr8:86514700..86563486hg19UCSC Ensembl
Innerchr8:86514715..86563472hg19UCSC Ensembl
Outerchr8:86514686..86563501hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3848787
hg1948787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13246111, essv13246112, essv13246113, essv13246115, essv13246114
SamplesNA19038, NA18557, HG03294, NA18634, HG02410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617886
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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