A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768668



Internal ID16062624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929590..18943568hg38UCSC Ensembl
Innerchr11:18951137..18965115hg19UCSC Ensembl
Innerchr11:18907713..18921691hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3813979
hg1913979
hg1813979
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553663
Supporting Variants
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768668
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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