A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841666



Internal ID22025309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48693532..48693532hg38UCSC Ensembl
chr10:49901577..49901577hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240642
Supporting Variants
Samples
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841666
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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