A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036877



Internal ID19126096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21470637..21524695hg38UCSC Ensembl
Innerchr11:21492183..21546241hg19UCSC Ensembl
Innerchr11:21448759..21502817hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3854059
hg1954059
hg1854059
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505563
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)nsv1036877
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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