A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14109142



Internal ID21277474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:151567185..151579767hg38UCSC Ensembl
Innerchr5:150946746..150959328hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg3812583
hg1912583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3118167
Supporting Variants
Samplessample252
Known GenesFAT2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14109142
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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