A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632080



Internal ID21580385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72928053..72928053hg38UCSC Ensembl
chr9:75542969..75542969hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162638
SamplesHG00732
Known GenesALDH1A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632080
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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