A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032259



Internal ID20599299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80215401..80216200hg38UCSC Ensembl
chr16:80249298..80250097hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498520
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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