A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14453389



Internal ID22248150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68449539..68452880hg38UCSC Ensembl
chr2:68676671..68680012hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg383342
hg193342
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181788
Supporting Variants
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14453389
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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