A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047389



Internal ID19136608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:81274905..81303874hg38UCSC Ensembl
Innerchr11:80985948..81014917hg19UCSC Ensembl
Innerchr11:80663596..80692565hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3828970
hg1928970
hg1828970
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1241n100
Supporting Variantsnssv3522206, nssv3511183
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)nsv1047389
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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