A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3537796



Internal ID22406992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32855876..32855876hg38UCSC Ensembl
chr5:32855982..32855982hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14399303, nssv14426645
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3537796
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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