A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561235



Internal ID22430016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:6355388..6355388hg38UCSC Ensembl
chr19:6355399..6355399hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291412, nssv14291411
SamplesNA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561235
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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