A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14408919



Internal ID22320024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12698689..12699025hg38UCSC Ensembl
chrUn_gl000235:6959..7295hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38337
hg19337
Variant TypeCNV alu deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188746
Supporting Variants
SamplesNA19240
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)nssv14408919
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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