A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186387



Internal ID20753427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77118701..77125300hg38UCSC Ensembl
chr13:77692836..77699435hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484585
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186387
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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