A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613963



Internal ID7000858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84287753..84307569hg38UCSC Ensembl
chr7:83917069..83936885hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3819817
hg1919817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1307e214
Supporting Variantsessv12875153, essv12875154
SamplesNA19397, HG02977
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613963
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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