A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17162638



Internal ID21443805
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 StatusS
Merged Variantsnsv5632080
Supporting Variants
SamplesHG00732
Known GenesALDH1A1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17162638
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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