A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291091



Internal ID22135561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1727029..1727293hg38UCSC Ensembl
chr19:1727028..1727292hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38265
hg19265
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222027
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291091
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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