A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032591



Internal ID20599631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81978401..81978800hg38UCSC Ensembl
chr16:82012006..82012405hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6507301
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032591
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.15678


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