A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617625



Internal ID7004510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72955608..72958357hg38UCSC Ensembl
Innerchr8:72955621..72958345hg38UCSC Ensembl
Outerchr8:72955596..72958370hg38UCSC Ensembl
chr8:73867843..73870592hg19UCSC Ensembl
Innerchr8:73867856..73870580hg19UCSC Ensembl
Outerchr8:73867831..73870605hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg382750
hg192750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13224821
SamplesHG01841
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617625
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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