A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5930943



Internal ID22706218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68195987..68196338hg38UCSC Ensembl
chr15:68488325..68488676hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17374328
Samples
Known GenesCALML4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5930943
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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