A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14368237



Internal ID22225967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:60358327..60358423hg38UCSC Ensembl
chr13:60932461..60932557hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527374
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14368237
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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