A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215060



Internal ID20782100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138865972..138869781hg38UCSC Ensembl
chr5:138201661..138205470hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg383810
hg193810
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6412072
Supporting Variants
Samples
Known GenesCTNNA1, LRRTM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215060
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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