A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225613



Internal ID22368688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66337937..66338003hg38UCSC Ensembl
chr9:42183748..42183802hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3867
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9576n152
Supporting Variantsnssv14439226, nssv14439749
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225613
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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