A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204551



Internal ID22353386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241546311..241546370hg38UCSC Ensembl
chr2:242485726..242485785hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5127n152
Supporting Variantsnssv14408412
SamplesNA19240
Known GenesBOK-AS1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204551
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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