A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4739262



Internal ID20515235
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 StatusM
Merged Variants
Supporting Variantsnssv16296453
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4739262
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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