A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16941607



Internal ID28426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159085574..159161574hg38UCSC Ensembl
chr3:158803363..158879363hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3876001
hg1976001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5450512
Supporting Variants
Samples
Known GenesIQCJ, IQCJ-SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16941607
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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