A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515494



Internal ID20888854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64726632..64754158hg38UCSC Ensembl
chr15:65018831..65046357hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3827527
hg1927527
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189209
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515494
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer