A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553667



Internal ID16341076
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 StatusM
Merged Variantsdgv1683n54
Supporting Variantsnssv768675, nssv768677, nssv768678, nssv768680, nssv768676, nssv768673, nssv768679, nssv768681, nssv768674
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553667
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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