A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14287035



Internal ID22200735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55159745..55159819hg38UCSC Ensembl
chr19:55671113..55671187hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3535616
Supporting Variants
SamplesHG00732
Known GenesDNAAF3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14287035
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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