A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560704



Internal ID333704
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 StatusM
Merged Variants
Supporting Variantsnssv16930854
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)nsv5560704
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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