A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14257420



Internal ID22200784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:61146061..61163610hg38UCSC Ensembl
Outerchr13:61720195..61737744hg19UCSC Ensembl
Cytoband13q21.2
Allele length
AssemblyAllele length
hg387421
hg197421
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3237039
Supporting Variants
SamplesHG00732
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14257420
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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