A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7034



Internal ID15536830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:131782594..131813566hg38UCSC Ensembl
Outerchr3:131501438..131532410hg19UCSC Ensembl
Outerchr3:132984128..133015100hg18UCSC Ensembl
Outerchr3:132984136..133015108hg17UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3830973
hg1930973
hg1830973
hg1730973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4007
Supporting Variants
SamplesNA12156
Known GenesCPNE4
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)nssv7034
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