A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5938155



Internal ID22713533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102410270..102411729hg38UCSC Ensembl
chr14:102876607..102878066hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17386879
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5938155
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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