A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3186836



Internal ID22339408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:14274478..14275373hg38UCSC Ensembl
chr2:14414602..14415497hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38896
hg19896
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4496n152
Supporting Variantsnssv14393582
SamplesNA19240
Known GenesLINC00276
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3186836
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer