A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5941499



Internal ID22716924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:26730662..26751529hg38UCSC Ensembl
chr13:27304799..27325666hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg3820868
hg1920868
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5941499
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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