A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735051



Internal ID158717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:14685624..14792914hg38UCSC Ensembl
chr4:14687248..14794538hg19UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg38107291
hg19107291
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5435725
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735051
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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