A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155969



Internal ID22086474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63142557..63150093hg38UCSC Ensembl
Outerchr3:63128733..63157334hg38UCSC Ensembl
Innerchr3:63128233..63135769hg19UCSC Ensembl
Outerchr3:63114409..63143010hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3828602
hg1928602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016392, nssv4016391
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155969
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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