A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5952902



Internal ID22728206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21833520..21833520hg38UCSC Ensembl
chr5:21833629..21833629hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412403
Samples
Known GenesCDH12
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5952902
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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