A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768677



Internal ID16062633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18930975..18938477hg38UCSC Ensembl
Innerchr11:18952522..18960024hg19UCSC Ensembl
Innerchr11:18909098..18916600hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387503
hg197503
hg187503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553667
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)nssv768677
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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