A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3210165



Internal ID22358126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:91536188..91536341hg38UCSC Ensembl
chr8:92548416..92548569hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14454220
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)nsv3210165
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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