A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046971



Internal ID19136190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18919311..18949616hg38UCSC Ensembl
Innerchr11:18940858..18971163hg19UCSC Ensembl
Innerchr11:18897434..18927739hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3830306
hg1930306
hg1830306
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515645
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)nsv1046971
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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