A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047474



Internal ID18790005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1803515..2043381hg38UCSC Ensembl
Innerchr11:1824745..2064611hg19UCSC Ensembl
Innerchr11:1781321..2021187hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38239867
hg19239867
hg18239867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518662
Samples
Known GenesH19, LSP1, MIR4298, MIR675, MRPL23, MRPL23-AS1, SYT8, TNNI2, TNNT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047474
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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