A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200362



Internal ID22349826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:34541260..34541310hg38UCSC Ensembl
chr13:35115397..35115447hg19UCSC Ensembl
Cytoband13q13.2
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14461594, nssv14426829
SamplesHG00733, HG00514
Known GenesLINC00457
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200362
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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