A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17032188



Internal ID89164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:22997378..22997429hg38UCSC Ensembl
chr10:23286307..23286358hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412305
Supporting Variants
Samples
Known GenesARMC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17032188
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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