A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181099



Internal ID20748139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77190241..77500977hg38UCSC Ensembl
chr13:77764376..78075112hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38310737
hg19310737
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476400
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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