A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033117



Internal ID89774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36013613..36040460hg38UCSC Ensembl
chr10:36302541..36329388hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3826848
hg1926848
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492523
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033117
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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