A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707154



Internal ID21228948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1857816..1857866hg38UCSC Ensembl
chr5:1857930..1857980hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811641
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707154
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.935484


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