A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14348933



Internal ID22147351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93046279..93046601hg38UCSC Ensembl
chr9:95808561..95808883hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211746
Supporting Variants
SamplesHG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14348933
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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