A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14463184



Internal ID22214417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:16762472..16763091hg38UCSC Ensembl
chr6:16762703..16763322hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3181207
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)nssv14463184
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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