A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13680226



Internal ID21202090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:183464341..183464406hg38UCSC Ensembl
chr4:184385494..184385559hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809849
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13680226
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.53125


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