A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609790



Internal ID6650019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:84136454..84141874hg38UCSC Ensembl
Innerchr6:84136490..84141838hg38UCSC Ensembl
Outerchr6:84136418..84141910hg38UCSC Ensembl
chr6:84846173..84851593hg19UCSC Ensembl
Innerchr6:84846209..84851557hg19UCSC Ensembl
Outerchr6:84846137..84851629hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg385421
hg195421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454090, essv12454091, essv12454092, essv12454093
SamplesHG04003, NA20866, HG03871, HG03944
Known GenesKIAA1009
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609790
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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