A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505884



Internal ID20879158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25435701..25442100hg38UCSC Ensembl
chr15:25680848..25687247hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187769
Samples
Known GenesUBE3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505884
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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