A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521213



Internal ID15448506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7103531..7166098hg38UCSC Ensembl
Innerchr19:7103542..7166109hg19UCSC Ensembl
Innerchr19:7054542..7117109hg18UCSC Ensembl
Innerchr19:7054542..7117109hg17UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3862568
hg1962568
hg1862568
hg1762568
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694424
Samples
Known GenesINSR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521213
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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