A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688749



Internal ID21210602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:105437112..105437112hg38UCSC Ensembl
chr12:105830890..105830890hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790527
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688749
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.125


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