A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691409



Internal ID115075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77289292..77393895hg38UCSC Ensembl
chr13:77863427..77968030hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38104604
hg19104604
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5511073
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691409
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000468


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