A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032188



Internal ID20599228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:79172099..79211207hg38UCSC Ensembl
chr16:79205996..79245104hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3839109
hg1939109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503185
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032188
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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