A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013187



Internal ID20580227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77114130..77114554hg38UCSC Ensembl
chr13:77688265..77688689hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6494968
Supporting Variants
Samples
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00066


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