A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048562



Internal ID19137781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18930134..18940804hg38UCSC Ensembl
Innerchr11:18951681..18962351hg19UCSC Ensembl
Innerchr11:18908257..18918927hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810671
hg1910671
hg1810671
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3518247
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)nsv1048562
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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