A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2984115



Internal ID15692228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:154144372..154195139hg38UCSC Ensembl
InnerchrX:153409846..153460630hg19UCSC Ensembl
InnerchrX:153063040..153113824hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3850768
hg1950785
hg1850785
Variant TypeCNV gain
Copy Number8
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515186
Supporting Variants
SamplesNA18855
Known GenesOPN1LW, OPN1MW, OPN1MW2
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2984115
Frequency
Sample Size2366
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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