A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14344591



Internal ID22211724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9018100..9024374hg38UCSC Ensembl
chr9:9018100..9024374hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg386275
hg196275
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217483
Supporting Variants
SamplesHG00732
Known GenesPTPRD
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14344591
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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