A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032889



Internal ID20599929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81513008..81513457hg38UCSC Ensembl
chr16:81546613..81547062hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502595
Supporting Variants
Samples
Known GenesCMIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032889
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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