A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5970555



Internal ID22745490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69300606..69300606hg38UCSC Ensembl
chr15:69592945..69592945hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377050
Samples
Known GenesPAQR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5970555
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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