A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2983190



Internal ID15720261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150972661..150973781hg38UCSC Ensembl
InnerchrX:150141134..150142254hg19UCSC Ensembl
InnerchrX:149891792..149892912hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381121
hg191121
hg181121
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515184
Supporting Variants
SamplesNA18991
Known Genes
MethodOligo aCGH
AnalysisADM2 threshold = 5
PlatformAgilent Eichler Human CNP 180K v3.0
Comments
ReferenceCampbell_et_al_2011
Pubmed ID21397061
Accession Number(s)nssv2983190
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