A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174171



Internal ID22332681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169334034..169334155hg38UCSC Ensembl
chr6:169734129..169734250hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14459002
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174171
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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