A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036388



Internal ID18778919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120524395..120556426hg38UCSC Ensembl
Innerchr11:120395104..120427135hg19UCSC Ensembl
Innerchr11:119900314..119932345hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3832032
hg1932032
hg1832032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3502883
Samples
Known GenesGRIK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036388
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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