A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048018



Internal ID19137237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18927513..18939538hg38UCSC Ensembl
Innerchr11:18949060..18961085hg19UCSC Ensembl
Innerchr11:18905636..18917661hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812026
hg1912026
hg1812026
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3511905, nssv3502765, nssv3708547
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)nsv1048018
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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