A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046744



Internal ID19135963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928697..18940179hg38UCSC Ensembl
Innerchr11:18950244..18961726hg19UCSC Ensembl
Innerchr11:18906820..18918302hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811483
hg1911483
hg1811483
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3508939, nssv3518639
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)nsv1046744
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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