A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613495



Internal ID7000391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65997021..66017413hg38UCSC Ensembl
Innerchr7:65997521..66016913hg38UCSC Ensembl
Outerchr7:65996021..66018413hg38UCSC Ensembl
chr7:65462008..65482400hg19UCSC Ensembl
Innerchr7:65462508..65481900hg19UCSC Ensembl
Outerchr7:65461008..65483400hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3820393
hg1920393
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12816588
SamplesNA11892
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613495
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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