A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8353



Internal ID15188825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:28599179..28639473hg38UCSC Ensembl
Outerchr7:28638797..28679090hg19UCSC Ensembl
Outerchr7:28605322..28645615hg18UCSC Ensembl
Outerchr7:28412037..28452330hg17UCSC Ensembl
Cytoband7p15.1
Allele length
AssemblyAllele length
hg3840295
hg1940294
hg1840294
hg1740294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5679
Supporting Variants
SamplesNA12156
Known GenesCREB5
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)nssv8353
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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