A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814513



Internal ID21259851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310322..3310380hg38UCSC Ensembl
chr6:3310556..3310614hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705303
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814513
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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