A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389420



Internal ID21046973
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 StatusM
Merged Variants
Supporting Variantsnssv18213908
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389420
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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