A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055078



Internal ID18797609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:9231310..9517330hg38UCSC Ensembl
Innerchr11:9252857..9538877hg19UCSC Ensembl
Innerchr11:9209433..9495453hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38286021
hg19286021
hg18286021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518089
Samples
Known GenesDENND5A, IPO7, LOC644656, SNORA23, TMEM41B, ZNF143
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055078
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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