A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479578



Internal ID21137131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83822650..83828720hg38UCSC Ensembl
chr14:84288994..84295064hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg386071
hg196071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022250
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479578
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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