A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178896



Internal ID22335252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:169937162..169937216hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3855
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14426233
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3178896
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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