A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3535616



Internal ID22404857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55159745..55159819hg38UCSC Ensembl
chr19:55671113..55671187hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4362n152
Supporting Variantsnssv14287036, nssv14287035
SamplesHG00732, HG00733
Known GenesDNAAF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3535616
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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