A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609259



Internal ID6996181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63356303..63367930hg38UCSC Ensembl
Innerchr6:63356303..63367930hg38UCSC Ensembl
Outerchr6:63355803..63368430hg38UCSC Ensembl
chr6:64066208..64077835hg19UCSC Ensembl
Innerchr6:64066208..64077835hg19UCSC Ensembl
Outerchr6:64065708..64078335hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3811628
hg1911628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12389794, essv12389793
SamplesNA18516, NA19116
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609259
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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