A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697299



Internal ID21219149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139511733..139511782hg38UCSC Ensembl
chr3:139230575..139230624hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2806811
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697299
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.109375


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