A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958456



Internal ID39619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174843863..175490971hg38UCSC Ensembl
chr4:175765014..176412122hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38647109
hg19647109
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5462641
Supporting Variants
Samples
Known GenesADAM29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958456
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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