A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17846438



Internal ID22030081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43862297..43862297hg38UCSC Ensembl
chr15:44154495..44154495hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6241996
Supporting Variants
Samples
Known GenesWDR76
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17846438
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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