A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613965



Internal ID7000860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84485015..84537879hg38UCSC Ensembl
Innerchr7:84485015..84537879hg38UCSC Ensembl
Outerchr7:84484515..84538379hg38UCSC Ensembl
chr7:84114331..84167195hg19UCSC Ensembl
Innerchr7:84114331..84167195hg19UCSC Ensembl
Outerchr7:84113831..84167695hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3852865
hg1952865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12875156
SamplesHG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613965
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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