A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678052



Internal ID21199909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46389364..46389413hg38UCSC Ensembl
chr19:46892621..46892670hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2799899
Supporting Variants
Samples
Known GenesPPP5C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678052
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.826087


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