A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041835



Internal ID19131054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18928697..18939770hg38UCSC Ensembl
Innerchr11:18950244..18961317hg19UCSC Ensembl
Innerchr11:18906820..18917893hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3811074
hg1911074
hg1811074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1067n100
Supporting Variantsnssv3710049
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)nsv1041835
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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