A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5967730



Internal ID22742665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70861402..70861402hg38UCSC Ensembl
chr15:71153741..71153741hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386087
Samples
Known GenesLRRC49
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5967730
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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