A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3610745



Internal ID6997662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:128698987..128842001hg38UCSC Ensembl
Innerchr6:128699015..128841973hg38UCSC Ensembl
Outerchr6:128698959..128842029hg38UCSC Ensembl
chr6:129020132..129163146hg19UCSC Ensembl
Innerchr6:129020160..129163118hg19UCSC Ensembl
Outerchr6:129020104..129163174hg19UCSC Ensembl
Cytoband6q22.33
Allele length
AssemblyAllele length
hg38143015
hg19143015
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12541348
SamplesHG02660
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3610745
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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