A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211871



Internal ID22359290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:84705737..84804517hg38UCSC Ensembl
Outerchr13:85279872..85378652hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3898781
hg1998781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14256516
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211871
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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