A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841476



Internal ID22025119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76463901..76463901hg38UCSC Ensembl
chr9:79078817..79078817hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38274
hg19274
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6257778
Supporting Variants
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841476
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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