A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044311



Internal ID19133530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929947..18949189hg38UCSC Ensembl
Innerchr11:18951494..18970736hg19UCSC Ensembl
Innerchr11:18908070..18927312hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3819243
hg1919243
hg1819243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1071n100
Supporting Variantsnssv3710051
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)nsv1044311
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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