A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14426829



Internal ID22167286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34541260..34541310hg38UCSC Ensembl
chr13:35115397..35115447hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3200362
Supporting Variants
SamplesHG00514
Known GenesLINC00457
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14426829
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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