A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703874



Internal ID21225682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138772759..138772833hg38UCSC Ensembl
chr5:138108448..138108522hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811126
Supporting Variants
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency1


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