A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050713



Internal ID18793244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76436041..76556073hg38UCSC Ensembl
Innerchr11:76147085..76267117hg19UCSC Ensembl
Innerchr11:75824733..75944765hg18UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38120033
hg19120033
hg18120033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3517228
Samples
Known GenesC11orf30
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050713
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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