A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036345



Internal ID18778876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20714867..20744994hg38UCSC Ensembl
Innerchr11:20736413..20766540hg19UCSC Ensembl
Innerchr11:20692989..20723116hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3830128
hg1930128
hg1830128
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502838
Samples
Known GenesNELL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036345
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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