A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561031



Internal ID22425107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48313365..48313365hg38UCSC Ensembl
chr15:48605562..48605562hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14380196, nssv14378406, nssv14389262
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561031
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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