A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12631302



Internal ID3356393
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611634
Supporting Variants
SamplesHG03009
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12631302
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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