A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513609



Internal ID290128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112655782..112672015hg38UCSC Ensembl
chr13:113310096..113326329hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3816234
hg1916234
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693733
Samples
Known GenesC13orf35
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513609
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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