A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108403



Internal ID21269419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:142106764..142111133hg38UCSC Ensembl
Innerchr5:141486329..141490698hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg384370
hg194370
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114854
Supporting Variants
Samplessample139
Known GenesNDFIP1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108403
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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