A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032954



Internal ID20599994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84156318..84156724hg38UCSC Ensembl
chr16:84189923..84190329hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6498505
Supporting Variants
Samples
Known GenesDNAAF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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