A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029696



Internal ID20596736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:47016501..47023400hg38UCSC Ensembl
chr16:47050412..47057311hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502167
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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