A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560755



Internal ID22429552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55586539..55586539hg38UCSC Ensembl
chr16:55620451..55620451hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14383458, nssv14379978, nssv14385823, nssv14392432
SamplesNA19238, NA19240, HG00513, HG00514
Known GenesLPCAT2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560755
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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