A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033648



Internal ID20600688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87652238..87655616hg38UCSC Ensembl
chr16:87685844..87689222hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383379
hg193379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514886
Supporting Variants
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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