A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210238



Internal ID22358191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49861026..49861078hg38UCSC Ensembl
chr15:50153223..50153275hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14404620
SamplesNA19240
Known GenesATP8B4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3210238
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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