A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14459002



Internal ID22252719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169334034..169334155hg38UCSC Ensembl
chr6:169734129..169734250hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3174171
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)nssv14459002
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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