A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047344



Internal ID18789875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4503263..4609510hg38UCSC Ensembl
Innerchr11:4524493..4630740hg19UCSC Ensembl
Innerchr11:4481069..4587316hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38106248
hg19106248
hg18106248
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518526
Samples
Known GenesC11orf40, OR52I1, OR52I2, OR52M1, TRIM68
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047344
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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