A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611634



Internal ID6998540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166384229..166391861hg38UCSC Ensembl
Innerchr6:166384265..166391826hg38UCSC Ensembl
Outerchr6:166384194..166391897hg38UCSC Ensembl
chr6:166797717..166805349hg19UCSC Ensembl
Innerchr6:166797753..166805314hg19UCSC Ensembl
Outerchr6:166797682..166805385hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg387633
hg197633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12631301, essv12631302
SamplesHG03009, HG00186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611634
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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