A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16296453



Internal ID20505671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8848769..8849001hg38UCSC Ensembl
chr9:8848769..8849001hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4739262
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16296453
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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