A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3541272



Internal ID22410382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11389734..11390086hg38UCSC Ensembl
chr19:11500410..11500762hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286000, nssv14285999, nssv14286001, nssv14285998
SamplesHG00512, NA19238, NA19240, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3541272
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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