A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182773



Internal ID22337276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170376151..170378915hg38UCSC Ensembl
chr6:170685239..170688003hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382765
hg192765
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14436693, nssv14436694
SamplesHG00514
Known GenesFAM120B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182773
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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