A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3618382



Internal ID7005264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109694827..109751454hg38UCSC Ensembl
Innerchr8:109694861..109751420hg38UCSC Ensembl
Outerchr8:109694793..109751488hg38UCSC Ensembl
chr8:110707056..110763683hg19UCSC Ensembl
Innerchr8:110707090..110763649hg19UCSC Ensembl
Outerchr8:110707022..110763717hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3856628
hg1956628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13285614
SamplesHG00367
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3618382
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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