A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156569



Internal ID22086970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107998386..108037365hg38UCSC Ensembl
Outerchr6:107991219..108043378hg38UCSC Ensembl
Innerchr6:108319590..108358569hg19UCSC Ensembl
Outerchr6:108312423..108364582hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3852160
hg1952160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022616
Samples
Known GenesOSTM1
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156569
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer