A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053607



Internal ID18796138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120670086..120931297hg38UCSC Ensembl
Innerchr11:120540795..120802006hg19UCSC Ensembl
Innerchr11:120046005..120307216hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38261212
hg19261212
hg18261212
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3520058
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)nsv1053607
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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