A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047641



Internal ID19136860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20903998..20925123hg38UCSC Ensembl
Innerchr11:20925544..20946669hg19UCSC Ensembl
Innerchr11:20882120..20903245hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821126
hg1921126
hg1821126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518834
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)nsv1047641
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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