A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14458941



Internal ID22252725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52898600..52898702hg38UCSC Ensembl
chr6:52763398..52763500hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3187292
Supporting Variants
SamplesHG00733
Known GenesGSTA3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14458941
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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