A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053939



Internal ID19143158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18903976..18939619hg38UCSC Ensembl
Innerchr11:18925523..18961166hg19UCSC Ensembl
Innerchr11:18882099..18917742hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3835644
hg1935644
hg1835644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521138
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)nsv1053939
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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