A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3205431



Internal ID22354120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:175266583..175266664hg38UCSC Ensembl
chr5:174693586..174693667hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7626n152
Supporting Variantsnssv14410976
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)nsv3205431
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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