A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768666



Internal ID16062622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18929590..18942188hg38UCSC Ensembl
Innerchr11:18951137..18963735hg19UCSC Ensembl
Innerchr11:18907713..18920311hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812599
hg1912599
hg1812599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553662
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)nssv768666
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer