A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040465



Internal ID19129684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37438111..37522870hg38UCSC Ensembl
Innerchr11:37459661..37544420hg19UCSC Ensembl
Innerchr11:37416237..37500996hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3884760
hg1984760
hg1884760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710085
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)nsv1040465
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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