A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701026



Internal ID124692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73490382..73490433hg38UCSC Ensembl
chr15:73782723..73782774hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5425876
Supporting Variants
Samples
Known GenesC15orf60
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701026
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000781


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