A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3187292



Internal ID22339648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:52898600..52898702hg38UCSC Ensembl
chr6:52763398..52763500hg19UCSC Ensembl
Cytoband6p12.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14458941
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)nsv3187292
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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