A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501626



Internal ID20874862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65074101..65078500hg38UCSC Ensembl
chr15:65366439..65370838hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg384400
hg194400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2566n223
Supporting Variantsnssv18178993
Samples
Known GenesKBTBD13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501626
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