A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16965349



Internal ID44215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43620599..43620649hg38UCSC Ensembl
chr5:43620701..43620751hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553885
Supporting Variants
Samples
Known GenesNNT
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16965349
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008276


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