A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361959



Internal ID21019512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:23193347..23376385hg38UCSC Ensembl
chr3:23234838..23417876hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38183039
hg19183039
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210425
Samples
Known GenesMIR548AC, UBE2E2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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