A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3532251



Internal ID22401581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211434216..211434216hg38UCSC Ensembl
chr1:211607558..211607558hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14377265, nssv14376819
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSee descriptions for individual calls in download files
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3532251
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