A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3281902



Internal ID22380231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167875962..167876098hg38UCSC Ensembl
chr2:168732472..168732608hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4886n152
Supporting Variantsnssv14408341
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3281902
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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