A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3510363



Internal ID18808644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18938568hg38UCSC Ensembl
Innerchr11:18940322..18960115hg19UCSC Ensembl
Innerchr11:18896898..18916691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819794
hg1919794
hg1819794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037620
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)nssv3510363
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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