A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042075



Internal ID18784606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63964982..64045692hg38UCSC Ensembl
Innerchr11:63732454..63813164hg19UCSC Ensembl
Innerchr11:63489030..63569740hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3880711
hg1980711
hg1880711
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508960
Samples
Known GenesCOX8A, MACROD1, OTUB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042075
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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