A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035499



Internal ID18778030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120527934..120575725hg38UCSC Ensembl
Innerchr11:120398643..120446434hg19UCSC Ensembl
Innerchr11:119903853..119951644hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3847792
hg1947792
hg1847792
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1290n100
Supporting Variantsnssv3503806
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)nsv1035499
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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