A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155956



Internal ID22086461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:26432979..26445694hg38UCSC Ensembl
Outerchr3:26430418..26450276hg38UCSC Ensembl
Innerchr3:26474470..26487185hg19UCSC Ensembl
Outerchr3:26471909..26491767hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3819859
hg1919859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4016336
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155956
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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