A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498395



Internal ID20871605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80057321..80090587hg38UCSC Ensembl
chr16:80091218..80124484hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3833267
hg1933267
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032246
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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