A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14399515



Internal ID22309890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15726212..15726311hg38UCSC Ensembl
chr6:15726443..15726542hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3183074
Supporting Variants
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14399515
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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