A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510780



Internal ID20884102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42999001..43020000hg38UCSC Ensembl
chr15:43291199..43312198hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3821000
hg1921000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195269
Samples
Known GenesUBR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510780
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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