A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171367



Internal ID22331251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238638056..238639444hg38UCSC Ensembl
chr2:239546697..239548085hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg381389
hg191389
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5079n152
Supporting Variantsnssv14394292
SamplesNA19240
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3171367
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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