A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565172



Internal ID22433893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20287079..20287079hg38UCSC Ensembl
chr8:20144590..20144590hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14340296, nssv14340298, nssv14340297
SamplesNA19238, NA19239, NA19240
Known GenesLZTS1-AS1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565172
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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