A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17594086



Internal ID21786129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72928053..72928053hg38UCSC Ensembl
chr9:75542969..75542969hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088047
Supporting Variants
Samples
Known GenesALDH1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17594086
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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