A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960702



Internal ID41108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187163381..187545381hg38UCSC Ensembl
chr4:188084535..188466535hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38382001
hg19382001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140478
Supporting Variants
Samples
Known GenesLOC339975
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960702
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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