A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039284



Internal ID18781815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:122985952..123083303hg38UCSC Ensembl
Innerchr11:122856660..122954011hg19UCSC Ensembl
Innerchr11:122361870..122459221hg18UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3897352
hg1997352
hg1897352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505777
Samples
Known GenesCLMP, HSPA8, LOC341056
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039284
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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