A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553669



Internal ID16341078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18931723..18938477hg38UCSC Ensembl
Innerchr11:18953270..18960024hg19UCSC Ensembl
Innerchr11:18909846..18916600hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg386755
hg196755
hg186755
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1683n54
Supporting Variantsnssv768689, nssv768687, nssv768685, nssv768683, nssv768686, nssv768684, nssv768688
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553669
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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