A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17691411



Internal ID115077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77318002..77318094hg38UCSC Ensembl
chr13:77892137..77892229hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5498778
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17691411
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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