A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14347018



Internal ID22279525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:79934084..79934201hg38UCSC Ensembl
chr9:82548999..82549116hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38118
hg19118
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3221035
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14347018
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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