A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553670



Internal ID16341079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18931723..18939601hg38UCSC Ensembl
Innerchr11:18953270..18961148hg19UCSC Ensembl
Innerchr11:18909846..18917724hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg387879
hg197879
hg187879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1683n54
Supporting Variantsnssv768692, nssv768690, nssv768691
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553670
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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