A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17450096



Internal ID22507966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67561131..67564247hg38UCSC Ensembl
chr10:69320889..69324005hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383117
hg193117
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852813
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17450096
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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