A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3112405



Internal ID21295671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96404938..96410502hg38UCSC Ensembl
Innerchr14:96871275..96876839hg19UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg385565
hg195565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14093981
Samplessample293
Known GenesAK7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3112405
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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