A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899072



Internal ID22674198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:19541278..19541331hg38UCSC Ensembl
chr5:19541387..19541440hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17428683
Samples
Known GenesCDH18
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899072
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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