A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687364



Internal ID21209219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20505745..20505900hg38UCSC Ensembl
chr14:20973904..20974059hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793247
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687364
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.117647


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