A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689225



Internal ID21211079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:93032308..93032426hg38UCSC Ensembl
chr15:93575538..93575656hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794676
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689225
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03125


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