A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524071



Internal ID22393500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67098160..67098160hg38UCSC Ensembl
chr4:67963878..67963878hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451838, nssv14398450
SamplesNA19240, HG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsInsertion of a AluY mobile element relative to the reference
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524071
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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