A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179902



Internal ID22335804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176746566..176746917hg38UCSC Ensembl
chr5:176173567..176173918hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14462631
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)nsv3179902
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer