A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042662



Internal ID19131881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18940259hg38UCSC Ensembl
Innerchr11:18940322..18961806hg19UCSC Ensembl
Innerchr11:18896898..18918382hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821485
hg1921485
hg1821485
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3512434
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)nsv1042662
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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