A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697230



Internal ID21219078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2226268..2226859hg38UCSC Ensembl
chr5:2226382..2226973hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811664
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697230
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.15625


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