A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215694



Internal ID20782734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:23650401..23734100hg38UCSC Ensembl
chr5:23650510..23734209hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3883700
hg1983700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375807
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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