A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032921



Internal ID20599961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8085001..8114600hg38UCSC Ensembl
chr16:8135003..8164602hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3829600
hg1929600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501802
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032921
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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