A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156786



Internal ID22087187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:153701198..153720772hg38UCSC Ensembl
Outerchr1:153699771..153722864hg38UCSC Ensembl
Innerchr1:153673674..153693248hg19UCSC Ensembl
Outerchr1:153672247..153695340hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3823094
hg1923094
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022955
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156786
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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