A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14291081



Internal ID22270482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1702512..1702603hg38UCSC Ensembl
chr19:1702511..1702602hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3214358
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14291081
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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