A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050954



Internal ID19140173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5875322..5914268hg38UCSC Ensembl
Innerchr11:5896552..5935498hg19UCSC Ensembl
Innerchr11:5853128..5892074hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3838947
hg1938947
hg1838947
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708502
Samples
Known GenesOR52E4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050954
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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