A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17031462



Internal ID88671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31987467..31998270hg38UCSC Ensembl
chr10:32276395..32287198hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3810804
hg1910804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5476841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17031462
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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