A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983970



Internal ID20551010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67264439..67265594hg38UCSC Ensembl
chr10:69024197..69025352hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448905
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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