A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16955007



Internal ID37317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:111690596..111809587hg38UCSC Ensembl
chr4:112611752..112730743hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38118992
hg19118992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5458421
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16955007
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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