A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514434



Internal ID20887787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25298439..25346015hg38UCSC Ensembl
chr15:25543586..25591162hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3847577
hg1947577
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185967
Samples
Known GenesUBE3A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514434
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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