A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094129



Internal ID21289932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103180431..103190865hg38UCSC Ensembl
Innerchr14:103646768..103657202hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3810435
hg1910435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117106
Supporting Variants
Samplessample53
Known GenesLINC00605
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094129
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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