A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591161



Internal ID16031884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:100631901..100699750hg38UCSC Ensembl
Innerchr3:100350745..100418594hg19UCSC Ensembl
Innerchr3:101833435..101901284hg18UCSC Ensembl
Cytoband3q12.2
Allele length
AssemblyAllele length
hg3867850
hg1967850
hg1867850
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8477n54
Supporting Variantsnssv970695, nssv970694, nssv970693
Samples
Known GenesGPR128
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591161
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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