A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182759



Internal ID22337264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:106498332..106498642hg38UCSC Ensembl
chr4:107419489..107419799hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14434813
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsAbsence of a AluY mobile element insertion that is present in the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182759
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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