A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611673



Internal ID6998579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167676520..167681200hg38UCSC Ensembl
Innerchr6:167676555..167681165hg38UCSC Ensembl
Outerchr6:167676485..167681235hg38UCSC Ensembl
chr6:168077200..168081880hg19UCSC Ensembl
Innerchr6:168077235..168081845hg19UCSC Ensembl
Outerchr6:168077165..168081915hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg384681
hg194681
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12643746
SamplesHG04035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611673
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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