A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225839



Internal ID22368848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:43998006..43998059hg38UCSC Ensembl
chr19:44502158..44502211hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286923
SamplesHG00731
Known GenesZNF155
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225839
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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