A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14369657



Internal ID22275885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98063851..98065700hg38UCSC Ensembl
chr13:98716105..98717954hg19UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg381850
hg191850
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220511
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14369657
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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