A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915909



Internal ID22691127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:9802488..9963922hg38UCSC Ensembl
chr9:9802488..9963922hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38161435
hg19161435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17432668
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915909
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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