A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213498



Internal ID20780538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42174756..42183402hg38UCSC Ensembl
chr5:42174858..42183504hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg388647
hg198647
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394647
Supporting Variants
Samples
Known GenesLOC101926960
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213498
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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