A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685880



Internal ID21207737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:39705753..39705914hg38UCSC Ensembl
chr4:39707373..39707534hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810896
Supporting Variants
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685880
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.4375


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