A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14415904



Internal ID22151492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84211854..84212044hg38UCSC Ensembl
chr13:84785989..84786179hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3197506
Supporting Variants
SamplesHG00514
Known GenesLINC00333
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14415904
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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