A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610595



Internal ID6997512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121640281..121649751hg38UCSC Ensembl
Innerchr6:121640288..121649745hg38UCSC Ensembl
Outerchr6:121640275..121649758hg38UCSC Ensembl
chr6:121961427..121970897hg19UCSC Ensembl
Innerchr6:121961434..121970891hg19UCSC Ensembl
Outerchr6:121961421..121970904hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg389471
hg199471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12526066, essv12526067, essv12526064, essv12526065, essv12526068
SamplesNA20531, HG00739, HG00332, HG00186, HG00372
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610595
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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