A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275507



Internal ID20484725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8484619..8484619hg38UCSC Ensembl
chr9:8484619..8484619hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4757508
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275507
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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