A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3867



Internal ID15548519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:70431207..70476246hg38UCSC Ensembl
Outerchr3:70480358..70525397hg19UCSC Ensembl
Outerchr3:70563048..70608087hg18UCSC Ensembl
Outerchr3:70563048..70608087hg17UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3845040
hg1945040
hg1845040
hg1745040
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7823
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)nsv3867
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