A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211519



Internal ID20778559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:179618883..179620444hg38UCSC Ensembl
chr3:179336671..179338232hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381562
hg191562
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375470
Supporting Variants
Samples
Known GenesNDUFB5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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