A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3236327



Internal ID22373547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:73162298..73162810hg38UCSC Ensembl
chr13:73736435..73736947hg19UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14366114, nssv14366115
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3236327
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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