A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969146



Internal ID22744081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32258752..32258752hg38UCSC Ensembl
chr13:32832889..32832889hg19UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17384058
Samples
Known GenesFRY
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969146
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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