A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180963



Internal ID22336329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26333427..26336722hg38UCSC Ensembl
chr2:26556295..26559590hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383296
hg193296
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4526n152
Supporting Variantsnssv14448359
SamplesHG00733
Known GenesGPR113
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3180963
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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