A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504260



Internal ID20877521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59091435..59133296hg38UCSC Ensembl
chr15:59383634..59425495hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3841862
hg1941862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191587
Samples
Known GenesCCNB2, RNF111
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504260
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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