A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608272



Internal ID6995202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:19400935..19403811hg38UCSC Ensembl
Innerchr6:19400971..19403775hg38UCSC Ensembl
Outerchr6:19400899..19403847hg38UCSC Ensembl
chr6:19401166..19404042hg19UCSC Ensembl
Innerchr6:19401202..19404006hg19UCSC Ensembl
Outerchr6:19401130..19404078hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382877
hg192877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12214119
SamplesHG02028
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608272
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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