A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177337



Internal ID22334368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166796769..166796821hg38UCSC Ensembl
chr6:167210257..167210309hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14390863
SamplesNA19240
Known GenesRPS6KA2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177337
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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