A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555903



Internal ID15996626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92907621..93144367hg38UCSC Ensembl
Innerchr11:92640787..92877533hg19UCSC Ensembl
Innerchr11:92280435..92517181hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38236747
hg19236747
hg18236747
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2094n54
Supporting Variantsnssv780933
Samples
Known GenesMTNR1B, SLC36A4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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