A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054501



Internal ID19143720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55006405..55172866hg38UCSC Ensembl
Innerchr11:54773881..54940342hg19UCSC Ensembl
Innerchr11:54530457..54696918hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38166462
hg19166462
hg18166462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1159n100
Supporting Variantsnssv3522194
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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