A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292232



Internal ID20501450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132377294..132377419hg38UCSC Ensembl
chr9:135252681..135252806hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4741603
Supporting Variants
Samples
Known GenesTTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292232
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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