A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14095047



Internal ID21282361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73536043..73568075hg38UCSC Ensembl
Innerchr14:74002747..74034779hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3832033
hg1932033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110845
Supporting Variants
Samplessample325
Known GenesACOT1, ACOT2, HEATR4
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14095047
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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