A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13691605



Internal ID21213456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41383303..41383480hg38UCSC Ensembl
chr15:41675501..41675678hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38178
hg19178
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795239
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13691605
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.166667


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