A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044093



Internal ID19133312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4522828..4567184hg38UCSC Ensembl
Innerchr11:4544058..4588414hg19UCSC Ensembl
Innerchr11:4500634..4544990hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3844357
hg1944357
hg1844357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513875
Samples
Known GenesOR52M1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044093
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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