A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611632



Internal ID6998538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166267954..166281187hg38UCSC Ensembl
Innerchr6:166267954..166281187hg38UCSC Ensembl
Outerchr6:166267454..166281687hg38UCSC Ensembl
chr6:166681442..166694675hg19UCSC Ensembl
Innerchr6:166681442..166694675hg19UCSC Ensembl
Outerchr6:166680942..166695175hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3813234
hg1913234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12631262
SamplesNA20845
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611632
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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