A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684991



Internal ID21206848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102998877..102999022hg38UCSC Ensembl
chr14:103465214..103465359hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793194
Supporting Variants
Samples
Known GenesCDC42BPB
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684991
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.983871


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