A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14437315



Internal ID22180517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87210391..87210724hg38UCSC Ensembl
chr9:89825306..89825639hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3222686
Supporting Variants
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)nssv14437315
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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