A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2814126



Internal ID21259465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3356066..3356066hg38UCSC Ensembl
chr6:3356300..3356300hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13709244
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2814126
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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