A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591153



Internal ID16031876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100616244..100719048hg38UCSC Ensembl
Innerchr3:100335088..100437892hg19UCSC Ensembl
Innerchr3:101817778..101920582hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg38102805
hg19102805
hg18102805
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8476n54
Supporting Variantsnssv970684, nssv970683
Samples
Known GenesGPR128, TFG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591153
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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