A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18028463



Internal ID20595503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14490619..14491367hg38UCSC Ensembl
chr16:14584476..14585224hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514905
Supporting Variants
Samples
Known GenesPARN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18028463
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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