A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17848697



Internal ID22032340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80985547..80985547hg38UCSC Ensembl
chr15:81277888..81277888hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6249864
Supporting Variants
Samples
Known GenesMESDC2
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17848697
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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