A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2793191



Internal ID21238529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102379631..102379681hg38UCSC Ensembl
chr14:102845968..102846018hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680895
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2793191
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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