A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156621



Internal ID22087022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169183828..169417906hg38UCSC Ensembl
Outerchr6:169180811..169421449hg38UCSC Ensembl
Innerchr6:169583923..169818001hg19UCSC Ensembl
Outerchr6:169580906..169821544hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38240639
hg19240639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022844
Samples
Known GenesTHBS2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156621
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