A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174753



Internal ID22332991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:20925697..20925810hg38UCSC Ensembl
chr8:20783208..20783321hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14453709
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174753
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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