A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17983216



Internal ID20550256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:66515690..66739039hg38UCSC Ensembl
chr10:68275448..68498797hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38223350
hg19223350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453413
Supporting Variants
Samples
Known GenesCTNNA3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17983216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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