A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2810896



Internal ID21256234
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 StatusM
Merged Variants
Supporting Variantsnssv13685880
Samples
Known GenesUBE2K
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2810896
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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