A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365556



Internal ID21023109
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 StatusM
Merged Variants
Supporting Variantsnssv18211486
Samples
Known GenesTBL1XR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365556
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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