A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033604



Internal ID20600644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87239477..87239924hg38UCSC Ensembl
chr16:87273083..87273530hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38448
hg19448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6502342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033604
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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