A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3172095



Internal ID22331637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:62102863..62104332hg38UCSC Ensembl
chr8:63015422..63016891hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg381470
hg191470
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9198n152
Supporting Variantsnssv14402794
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)nsv3172095
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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