A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5937665



Internal ID22713036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:70533334..70636334hg38UCSC Ensembl
chr13:71107466..71210466hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38103001
hg19103001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386134
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5937665
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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