A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210812



Internal ID20777852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9495638..9874055hg38UCSC Ensembl
chr3:9537322..9915739hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38378418
hg19378418
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362532
Supporting Variants
Samples
Known GenesARPC4, ARPC4-TTLL3, BRPF1, CAMK1, CIDEC, CPNE9, LHFPL4, MTMR14, OGG1, RPUSD3, TADA3, TTLL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210812
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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