A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17850409



Internal ID22034052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10175070..10175070hg38UCSC Ensembl
chr20:10155718..10155718hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6251234
Supporting Variants
Samples
Known GenesSNAP25-AS1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17850409
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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