A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14452870



Internal ID22247714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170397553..170401282hg38UCSC Ensembl
chr6:170706641..170710370hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg383730
hg193730
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3179749
Supporting Variants
SamplesHG00733
Known GenesFAM120B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14452870
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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