A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943145



Internal ID22718589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40656221..40666452hg38UCSC Ensembl
chr15:40948419..40958650hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3810232
hg1910232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17373978
Samples
Known GenesCASC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943145
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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