A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960720



Internal ID41120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187280385..188645059hg38UCSC Ensembl
chr4:188201539..189566213hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg381364675
hg191364675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5465669
Supporting Variants
Samples
Known GenesLINC01060, LOC339975, TRIML1, TRIML2, ZFP42
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960720
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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