A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2805906



Internal ID15595716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73530495..73532471hg38UCSC Ensembl
Innerchr14:73997199..73999175hg19UCSC Ensembl
Innerchr14:73066952..73068928hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381977
hg191977
hg181977
Variant TypeCNV gain
Copy Number5
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514746
Supporting Variants
SamplesNA07347
Known GenesHEATR4
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2805906
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer