A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560931



Internal ID22429726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62975200..62975200hg38UCSC Ensembl
chr16:63009104..63009104hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375586, nssv14381393, nssv14382706
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560931
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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