A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609787



Internal ID6996707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84024885..84029574hg38UCSC Ensembl
Innerchr6:84024885..84029574hg38UCSC Ensembl
Outerchr6:84024629..84029799hg38UCSC Ensembl
chr6:84734604..84739293hg19UCSC Ensembl
Innerchr6:84734604..84739293hg19UCSC Ensembl
Outerchr6:84734348..84739518hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg384690
hg194690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454085, essv12454082, essv12454083, essv12454081, essv12454087, essv12454080, essv12454086, essv12454084
SamplesHG02756, HG03079, HG01072, HG02502, NA19184, HG03060, HG03445, NA19129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609787
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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