A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13703307



Internal ID21225119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150366629..150366954hg38UCSC Ensembl
chr5:149746192..149746517hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810558
Supporting Variants
Samples
Known GenesTCOF1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13703307
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.703125


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