A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180902



Internal ID22336299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166858895..166858956hg38UCSC Ensembl
chr6:167272383..167272444hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14378345, nssv14462647, nssv14435771
SamplesNA19240, HG00733, HG00514
Known GenesRPS6KA2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180902
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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