A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029986



Internal ID20597026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:49814121..49814826hg38UCSC Ensembl
chr16:49848032..49848737hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502464
Supporting Variants
Samples
Known GenesZNF423
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00454


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