A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5894889



Internal ID22669965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196334807..196335088hg38UCSC Ensembl
chr3:196061678..196061959hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38282
hg19282
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17412512
Samples
Known GenesTM4SF19, TM4SF19-TCTEX1D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5894889
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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