A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909573



Internal ID22684783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65018599..65376171hg38UCSC Ensembl
chr10:66778357..67135929hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38357573
hg19357573
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909573
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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