A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644688



Internal ID21592993
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 Variantsnssv17087319
SamplesHG00731
Known GenesLRRC49
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644688
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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