A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944689



Internal ID22720158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:65354658..65932802hg38UCSC Ensembl
chr13:65928790..66506934hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg38578145
hg19578145
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389557
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944689
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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