A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681020



Internal ID21202883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:930050..930108hg38UCSC Ensembl
chr16:980050..980108hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2796451
Supporting Variants
Samples
Known GenesLMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681020
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.387097


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