A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17538435



Internal ID21862790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:38710019..38715563hg38UCSC Ensembl
chr3:38751510..38757054hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg385545
hg195545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5993360
Supporting Variants
Samples
Known GenesSCN10A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17538435
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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