A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3786



Internal ID15548430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:43814112..43843443hg38UCSC Ensembl
Outerchr3:43855604..43884935hg19UCSC Ensembl
Outerchr3:43830608..43859939hg18UCSC Ensembl
Outerchr3:43830608..43859939hg17UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg3829332
hg1929332
hg1829332
hg1729332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7798
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv3786
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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