A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8510



Internal ID15188668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:70276999..70321885hg38UCSC Ensembl
Outerchr8:71189234..71234120hg19UCSC Ensembl
Outerchr8:71351788..71396674hg18UCSC Ensembl
Outerchr8:71351788..71396674hg17UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3844887
hg1944887
hg1844887
hg1744887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6248
Supporting Variants
SamplesNA12156
Known GenesNCOA2
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)nssv8510
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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