A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560471



Internal ID22429268
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 Variantsnssv14389626, nssv14373114, nssv14376111, nssv14373797
SamplesHG00731, HG00733, HG00513, HG00514
Known GenesLRRC49
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560471
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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