A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3200721



Internal ID22350130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:89471699..89471795hg38UCSC Ensembl
chr9:92086614..92086710hg19UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14439562, nssv14439080, nssv14384204
SamplesNA19240, HG00733, HG00514
Known GenesSEMA4D
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3200721
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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