A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17386879



Internal ID22444749
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 StatusS
Merged Variantsnsv5938155
Supporting Variants
Samples
Known GenesTECPR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17386879
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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