A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14425922



Internal ID22166050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13925069..13925262hg38UCSC Ensembl
chr6:13925300..13925493hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg38194
hg19194
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171602
Supporting Variants
SamplesHG00514
Known GenesRNF182
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14425922
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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