A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048260



Internal ID19137479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18914707..18938568hg38UCSC Ensembl
Innerchr11:18936254..18960115hg19UCSC Ensembl
Innerchr11:18892830..18916691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3823862
hg1923862
hg1823862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1061n100
Supporting Variantsnssv3510718
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)nsv1048260
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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