A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033347



Internal ID89921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27871040..27879740hg38UCSC Ensembl
chr10:28159969..28168669hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg388701
hg198701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475278
Supporting Variants
Samples
Known GenesARMC4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033347
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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