A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18138359



Internal ID20705399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13777221..13857279hg38UCSC Ensembl
chr6:13777453..13857510hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg3880059
hg1980058
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415170
Supporting Variants
Samples
Known GenesMCUR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18138359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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