A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110932



Internal ID21294198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:36514721..36521443hg38UCSC Ensembl
Innerchr14:36983926..36990648hg19UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg386723
hg196723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14095571
Samplessample224
Known GenesNKX2-1, NKX2-1-AS1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110932
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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