A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609419



Internal ID6996340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:69668202..69669259hg38UCSC Ensembl
Innerchr6:69668202..69669259hg38UCSC Ensembl
Outerchr6:69667916..69669525hg38UCSC Ensembl
chr6:70378094..70379151hg19UCSC Ensembl
Innerchr6:70378094..70379151hg19UCSC Ensembl
Outerchr6:70377808..70379417hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg381058
hg191058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12410826
SamplesHG00657
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609419
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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