A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044861



Internal ID19134080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18931430..18949854hg38UCSC Ensembl
Innerchr11:18952977..18971401hg19UCSC Ensembl
Innerchr11:18909553..18927977hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3818425
hg1918425
hg1818425
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1071n100
Supporting Variantsnssv3511374
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)nsv1044861
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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