A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196105



Internal ID22346174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:107105175..107105227hg38UCSC Ensembl
chr8:108117403..108117455hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14429279
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196105
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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