A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156006



Internal ID22086511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:103172952..103267382hg38UCSC Ensembl
Outerchr3:103169105..103267957hg38UCSC Ensembl
Innerchr3:102891796..102986226hg19UCSC Ensembl
Outerchr3:102887949..102986801hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3898853
hg1998853
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017809
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156006
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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