A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051137



Internal ID19140356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37037236..37060975hg38UCSC Ensembl
Innerchr11:37058786..37082525hg19UCSC Ensembl
Innerchr11:37015362..37039101hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3823740
hg1923740
hg1823740
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3513596
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)nsv1051137
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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