A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2906585



Internal ID15670526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:67927799..67967407hg38UCSC Ensembl
Innerchr4:68793517..68833125hg19UCSC Ensembl
Innerchr4:68476112..68515720hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3839609
hg1939609
hg1839609
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv514221
Supporting Variants
SamplesNA18517
Known GenesTMPRSS11A
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2906585
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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