A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3225413



Internal ID22368549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15442083..15442271hg38UCSC Ensembl
chr9:15442081..15442269hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14345372
SamplesHG00732
Known GenesSNAPC3
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3225413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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