A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563960



Internal ID22395417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109886572..109886572hg38UCSC Ensembl
chr6:110207775..110207775hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14330838, nssv14330837
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563960
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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