A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211512



Internal ID22359049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94686913..94687169hg38UCSC Ensembl
chr9:97449195..97449451hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38257
hg19257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348996
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211512
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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