A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156009



Internal ID22086514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108012699..108025631hg38UCSC Ensembl
Outerchr3:108007306..108028167hg38UCSC Ensembl
Innerchr3:107731546..107744478hg19UCSC Ensembl
Outerchr3:107726153..107747014hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg3820862
hg1920862
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4017813
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156009
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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