A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610692



Internal ID6650918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:125594913..125598997hg38UCSC Ensembl
Innerchr6:125594923..125598988hg38UCSC Ensembl
Outerchr6:125594904..125599007hg38UCSC Ensembl
chr6:125916059..125920143hg19UCSC Ensembl
Innerchr6:125916069..125920134hg19UCSC Ensembl
Outerchr6:125916050..125920153hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg384085
hg194085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12537209
SamplesHG03270
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610692
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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