A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591248



Internal ID16378657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106961072..107003955hg38UCSC Ensembl
Innerchr3:106679919..106722802hg19UCSC Ensembl
Innerchr3:108162609..108205492hg18UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3842884
hg1942884
hg1842884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152520
SamplesHGDP00610
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591248
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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