A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532900



Internal ID22402222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:65739039..65739039hg38UCSC Ensembl
chr5:65034866..65034866hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14457944
SamplesHG00733
Known GenesNLN
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)nsv3532900
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer