A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5975413



Internal ID22750348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72702802..72702802hg38UCSC Ensembl
chr15:72995143..72995143hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38225
hg19225
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379745
Samples
Known GenesBBS4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5975413
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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