A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3178162



Internal ID22334836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31823409..31825430hg38UCSC Ensembl
chr2:32048478..32050499hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg382022
hg192022
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4540n152
Supporting Variantsnssv14395238
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)nsv3178162
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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