A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518403



Internal ID18816684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928314..18940179hg38UCSC Ensembl
Innerchr11:18949861..18961726hg19UCSC Ensembl
Innerchr11:18906437..18918302hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811866
hg1911866
hg1811866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048735
Supporting Variants
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518403
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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