A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613959



Internal ID7000854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84208869..84243049hg38UCSC Ensembl
Innerchr7:84208869..84243049hg38UCSC Ensembl
Outerchr7:84208369..84243549hg38UCSC Ensembl
chr7:83838185..83872365hg19UCSC Ensembl
Innerchr7:83838185..83872365hg19UCSC Ensembl
Outerchr7:83837685..83872865hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3834181
hg1934181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12875061
SamplesHG04054
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613959
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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