A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046266



Internal ID19135485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18919311..18938568hg38UCSC Ensembl
Innerchr11:18940858..18960115hg19UCSC Ensembl
Innerchr11:18897434..18916691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819258
hg1919258
hg1819258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1064n100
Supporting Variantsnssv3520990, nssv3508293
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)nsv1046266
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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