A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3285310



Internal ID22383687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119063169..119063224hg38UCSC Ensembl
chr5:118398864..118398919hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14410628
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3285310
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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