A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5933261



Internal ID22708571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:42275684..42275865hg38UCSC Ensembl
chr13:42849820..42850001hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383160
Samples
Known GenesAKAP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5933261
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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