A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608666



Internal ID6995590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:34611728..34612852hg38UCSC Ensembl
Innerchr6:34611778..34612802hg38UCSC Ensembl
Outerchr6:34611630..34612950hg38UCSC Ensembl
chr6:34579505..34580629hg19UCSC Ensembl
Innerchr6:34579555..34580579hg19UCSC Ensembl
Outerchr6:34579407..34580727hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg381125
hg191125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12313494, essv12313493
SamplesNA20589, NA19072
Known GenesC6orf106
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608666
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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