A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036655



Internal ID19125874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18939191hg38UCSC Ensembl
Innerchr11:18940322..18960738hg19UCSC Ensembl
Innerchr11:18896898..18917314hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820417
hg1920417
hg1820417
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3505345
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)nsv1036655
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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