A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052776



Internal ID19141995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:112472187..112509310hg38UCSC Ensembl
Innerchr11:112342910..112380033hg19UCSC Ensembl
Innerchr11:111848120..111885243hg18UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3837124
hg1937124
hg1837124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710749, nssv3513655, nssv3504516, nssv3514294
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052776
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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