A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044744



Internal ID19133963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18940363hg38UCSC Ensembl
Innerchr11:18940322..18961910hg19UCSC Ensembl
Innerchr11:18896898..18918486hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821589
hg1921589
hg1821589
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1063n100
Supporting Variantsnssv3506576, nssv3519825, nssv3516577
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)nsv1044744
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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