A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202118



Internal ID22351323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49652608..49652673hg38UCSC Ensembl
chr15:49944805..49944870hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14381220
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202118
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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