A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373830



Internal ID22297716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170397682..170400987hg38UCSC Ensembl
chr6:170706770..170710075hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383306
hg193306
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3171206
Supporting Variants
SamplesNA19240
Known GenesFAM120B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373830
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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