A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14094378



Internal ID21288655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:51500904..51903447hg38UCSC Ensembl
Innerchr13:52075040..52477583hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38402544
hg19402544
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3113028
Supporting Variants
Samplessample42
Known GenesCCDC70, DHRS12, LINC00282, MIR4703, WDFY2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14094378
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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