A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5931781



Internal ID22707070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37885681..37885755hg38UCSC Ensembl
chr13:38459818..38459892hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17370402
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5931781
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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