A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617005



Internal ID7003891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:42226144..42255022hg38UCSC Ensembl
Innerchr8:42226144..42255022hg38UCSC Ensembl
Outerchr8:42225644..42255522hg38UCSC Ensembl
chr8:42083662..42112540hg19UCSC Ensembl
Innerchr8:42083662..42112540hg19UCSC Ensembl
Outerchr8:42083162..42113040hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3828879
hg1928879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13183746
SamplesHG01177
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617005
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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