A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3183189



Internal ID22337489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24683759..24684456hg38UCSC Ensembl
chr6:24683987..24684684hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38698
hg19698
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7785n152
Supporting Variantsnssv14464400, nssv14425802
SamplesHG00733, HG00514
Known GenesACOT13
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3183189
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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