A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14466402



Internal ID22215501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16950603..16950707hg38UCSC Ensembl
chr6:16950834..16950938hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38105
hg19105
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181674
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)nssv14466402
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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