A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053898



Internal ID19143117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:109204800..109270255hg38UCSC Ensembl
Innerchr11:109075527..109140982hg19UCSC Ensembl
Innerchr11:108580737..108646192hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3865456
hg1965456
hg1865456
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520346
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)nsv1053898
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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