A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201566



Internal ID22350848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101910373..101910523hg38UCSC Ensembl
chr8:102922601..102922751hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38151
hg19151
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9277n152
Supporting Variantsnssv14461615
SamplesHG00733
Known GenesNCALD
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201566
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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