A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508583



Internal ID20881886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82507658..82572465hg38UCSC Ensembl
chr16:82541263..82606070hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3864808
hg1964808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032666
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508583
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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