A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7794



Internal ID15189384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:41292209..41337232hg38UCSC Ensembl
Outerchr3:41333700..41378723hg19UCSC Ensembl
Outerchr3:41308704..41353727hg18UCSC Ensembl
Outerchr3:41308704..41353727hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3845024
hg1945024
hg1845024
hg1745024
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3779
Supporting Variants
SamplesNA12156
Known GenesULK4
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)nssv7794
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