A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945084



Internal ID30718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8605162..8605595hg38UCSC Ensembl
chr4:8606889..8607322hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5553104
Supporting Variants
Samples
Known GenesCPZ
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945084
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109978


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