A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13682597



Internal ID21204454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:18161050..18161050hg38UCSC Ensembl
chr4:18162673..18162673hg19UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg381499
hg191499
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13682597
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.515625


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