A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14443669



Internal ID22239753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:18339158..18340758hg38UCSC Ensembl
chrUn_gl000212:167910..169510hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381601
hg191601
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3193459
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)nssv14443669
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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