A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196967



Internal ID22346899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:110827155..110827254hg38UCSC Ensembl
chr13:111479502..111479601hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454944
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196967
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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