A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3530977



Internal ID22400344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19513108..19513640hg38UCSC Ensembl
chr19:19623917..19624449hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4174n152
Supporting Variantsnssv14287272
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3530977
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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