A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17428708



Internal ID22486578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:11165965..11176910hg38UCSC Ensembl
chr5:11166077..11177022hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3810946
hg1910946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5899344
Supporting Variants
Samples
Known GenesCTNND2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17428708
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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