A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18213908



Internal ID20780948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15373074..15373723hg38UCSC Ensembl
chr5:15373183..15373832hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6389420
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18213908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00023


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