A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054089



Internal ID19143308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134977634..135074876hg38UCSC Ensembl
Innerchr11:134847528..134944770hg19UCSC Ensembl
Innerchr11:134352738..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3897243
hg1997243
hg1897245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3519851, nssv3710797
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)nsv1054089
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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