A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818103



Internal ID21263441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22585636..22585636hg38UCSC Ensembl
chr8:22443149..22443149hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710737
Samples
Known GenesPDLIM2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818103
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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