A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029183



Internal ID87151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11805142..11860066hg38UCSC Ensembl
chr10:11847141..11902065hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3854925
hg1954925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5479321
Supporting Variants
Samples
Known GenesPROSER2, PROSER2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029183
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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