A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17033011



Internal ID89709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:33377273..34316186hg38UCSC Ensembl
chr10:33666201..34605114hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38938914
hg19938914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491167
Supporting Variants
Samples
Known GenesLINC00838, PARD3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17033011
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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