A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702361



Internal ID126027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:70861402..70861402hg38UCSC Ensembl
chr15:71153741..71153741hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5421788
Supporting Variants
Samples
Known GenesLRRC49
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702361
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.26813


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