A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199018



Internal ID22348666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:42896121..42896234hg38UCSC Ensembl
chr9:44074885..44074998hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439205
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)nsv3199018
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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