A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527268



Internal ID22396655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2033041..2033184hg38UCSC Ensembl
chr19:2033040..2033183hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14291106, nssv14291107, nssv14291105
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527268
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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