A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13709010



Internal ID21230793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:6977630..6977709hg38UCSC Ensembl
chr4:6979357..6979436hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809606
Supporting Variants
Samples
Known GenesTBC1D14
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13709010
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.692308


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