A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214032



Internal ID22360798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:13853851..13854307hg38UCSC Ensembl
chr19:13964665..13965121hg19UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg38457
hg19457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14286081, nssv14286082
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214032
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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