A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177879



Internal ID22334675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:168309447..168309505hg38UCSC Ensembl
chr6:168710127..168710185hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14426623
SamplesHG00514
Known GenesDACT2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3177879
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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