A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029773



Internal ID20596813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57132898..57133355hg38UCSC Ensembl
chr16:57166810..57167267hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501037
Supporting Variants
Samples
Known GenesCPNE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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