A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029442



Internal ID20596482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24025931..24030179hg38UCSC Ensembl
chr16:24037252..24041500hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg384249
hg194249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6499519
Supporting Variants
Samples
Known GenesPRKCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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