A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180618



Internal ID22336154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144149611..144149711hg38UCSC Ensembl
chr6:144470748..144470848hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399613
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)nsv3180618
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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