A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13711563



Internal ID21233319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79966893..79972937hg38UCSC Ensembl
chr4:80888047..80894091hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg386045
hg196045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811255
Supporting Variants
Samples
Known GenesANTXR2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13711563
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.796875


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