A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032219



Internal ID20599259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7970916..8179414hg38UCSC Ensembl
chr16:8020918..8229416hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38208499
hg19208499
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6500189
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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