A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033471



Internal ID90003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29088125..29109685hg38UCSC Ensembl
chr10:29377054..29398614hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3821561
hg1921561
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481369
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033471
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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