A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050843



Internal ID19140062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918534..18940094hg38UCSC Ensembl
Innerchr11:18940081..18961641hg19UCSC Ensembl
Innerchr11:18896657..18918217hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821561
hg1921561
hg1821561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3517379
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)nsv1050843
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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