A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201843



Internal ID22351089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64118992..64119200hg38UCSC Ensembl
chr15:64411191..64411399hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378319
SamplesNA19240
Known GenesSNX1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201843
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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