A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211486



Internal ID20778526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176987326..177158241hg38UCSC Ensembl
chr3:176705114..176876029hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg38170916
hg19170916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6365556
Supporting Variants
Samples
Known GenesTBL1XR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211486
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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