A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156496



Internal ID22086897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40012620..40252367hg38UCSC Ensembl
Outerchr6:40007552..40253287hg38UCSC Ensembl
Innerchr6:39980359..40220106hg19UCSC Ensembl
Outerchr6:39975291..40221026hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg38245736
hg19245736
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4018553
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156496
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