A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974104



Internal ID50112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138934774..138945833hg38UCSC Ensembl
chr5:138270463..138281522hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3811060
hg1911060
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563509
Supporting Variants
Samples
Known GenesCTNNA1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974104
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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