A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6240642



Internal ID22045252
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 StatusM
Merged Variants
Supporting Variantsnssv17841666
Samples
Known GenesWDFY4
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6240642
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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