A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609013



Internal ID6649246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52901914..52922345hg38UCSC Ensembl
Innerchr6:52901916..52922344hg38UCSC Ensembl
Outerchr6:52901913..52922347hg38UCSC Ensembl
chr6:52766712..52787143hg19UCSC Ensembl
Innerchr6:52766714..52787142hg19UCSC Ensembl
Outerchr6:52766711..52787145hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg3820432
hg1920432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12353979, essv12353978, essv12353977
SamplesHG04022, HG02728, HG03727
Known GenesGSTA3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609013
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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