A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818087



Internal ID21263425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17552513..17552598hg38UCSC Ensembl
chr8:17410022..17410107hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710284
Samples
Known GenesSLC7A2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818087
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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