A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14426544



Internal ID22166958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:123099040..123099120hg38UCSC Ensembl
chr6:123420185..123420265hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3188105
Supporting Variants
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14426544
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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