A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379485



Internal ID21037038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17902593..17915582hg38UCSC Ensembl
chr5:17902702..17915691hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3812990
hg1912990
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215123
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379485
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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