A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044319



Internal ID19133538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18919311..18940149hg38UCSC Ensembl
Innerchr11:18940858..18961696hg19UCSC Ensembl
Innerchr11:18897434..18918272hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3820839
hg1920839
hg1820839
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1064n100
Supporting Variantsnssv3514099
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)nsv1044319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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