A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170381



Internal ID22330718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239124645..239124734hg38UCSC Ensembl
chr2:240046341..240046430hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14394308
SamplesNA19240
Known GenesHDAC4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170381
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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