A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036064



Internal ID19125283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18917623..18940363hg38UCSC Ensembl
Innerchr11:18939170..18961910hg19UCSC Ensembl
Innerchr11:18895746..18918486hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3822741
hg1922741
hg1822741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3503314
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)nsv1036064
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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