A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3194213



Internal ID22344559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:2115941..2116008hg38UCSC Ensembl
chr20:2096587..2096654hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14395492
SamplesNA19240
Known GenesSTK35
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3194213
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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