A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051211



Internal ID18793742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:26451584..26583006hg38UCSC Ensembl
Innerchr11:26473131..26604553hg19UCSC Ensembl
Innerchr11:26429707..26561129hg18UCSC Ensembl
Cytoband11p14.2
Allele length
AssemblyAllele length
hg38131423
hg19131423
hg18131423
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710070
Samples
Known GenesANO3, MUC15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051211
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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