A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6088047



Internal ID21997280
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 StatusM
Merged Variants
Supporting Variantsnssv17594086
Samples
Known GenesALDH1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6088047
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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