A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156639



Internal ID22087040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:9756036..9996166hg38UCSC Ensembl
Outerchr7:9752495..10010274hg38UCSC Ensembl
Innerchr7:9795665..10035793hg19UCSC Ensembl
Outerchr7:9792124..10049901hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38257780
hg19257778
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021047
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156639
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