A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686063



Internal ID21207917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59233685..59233685hg38UCSC Ensembl
chr18:56900917..56900917hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2798127
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686063
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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