A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029953



Internal ID20596993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4911448..4916409hg38UCSC Ensembl
chr16:4961449..4966410hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg384962
hg194962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495889
Supporting Variants
Samples
Known GenesPPL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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