A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281532



Internal ID20490750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:9624549..9624549hg38UCSC Ensembl
chr20:9605196..9605196hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754009
Supporting Variants
Samples
Known GenesPAK7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281532
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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