A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3540847



Internal ID22409972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:75239128..75239128hg38UCSC Ensembl
chr5:74534953..74534953hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399065
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)nsv3540847
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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