A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17381903



Internal ID22439773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:78144082..78314241hg38UCSC Ensembl
chr16:78177979..78348138hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38170160
hg19170160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936104
Supporting Variants
Samples
Known GenesWWOX
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17381903
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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