A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214115



Internal ID20781155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43504101..43512000hg38UCSC Ensembl
chr5:43504203..43512102hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg387900
hg197900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6377403
Supporting Variants
Samples
Known GenesC5orf34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214115
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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