A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214123



Internal ID20781163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43965495..43976183hg38UCSC Ensembl
chr5:43965597..43976285hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3810689
hg1910689
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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