A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525417



Internal ID21849775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:11167131..11167265hg38UCSC Ensembl
chr3:11208817..11208951hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5990991
Supporting Variants
Samples
Known GenesHRH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525417
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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