A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560764



Internal ID22429561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75621256..75621256hg38UCSC Ensembl
chr16:75655154..75655154hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386233, nssv14379749
SamplesHG00512, HG00514
Known GenesADAT1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560764
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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