A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155556



Internal ID22086061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15565939..15586386hg38UCSC Ensembl
Outerchr19:15560084..15590267hg38UCSC Ensembl
Innerchr19:15676750..15697197hg19UCSC Ensembl
Outerchr19:15670895..15701078hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3830184
hg1930184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4013457
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155556
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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