A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16930854



Internal ID21322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9765591..9883063hg38UCSC Ensembl
chr3:9807275..9924747hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38117473
hg19117473
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560704
Supporting Variants
Samples
Known GenesARPC4, ARPC4-TTLL3, CAMK1, CIDEC, OGG1, RPUSD3, TADA3, TTLL3
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16930854
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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