A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6159



Internal ID15551040
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:37263987..37309470hg38UCSC Ensembl
Outerchr8:37121505..37166988hg19UCSC Ensembl
Outerchr8:37240663..37286146hg18UCSC Ensembl
Outerchr8:37240663..37286146hg17UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg3845484
hg1945484
hg1845484
hg1745484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6214
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)nsv6159
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