A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3179631



Internal ID22335657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26333427..26336723hg38UCSC Ensembl
chr2:26556295..26559591hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383297
hg193297
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4526n152
Supporting Variantsnssv14395210
SamplesNA19240
Known GenesGPR113
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3179631
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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