A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6168



Internal ID15204364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:42092972..42137630hg38UCSC Ensembl
Outerchr8:41950490..41995148hg19UCSC Ensembl
Outerchr8:42069647..42114305hg18UCSC Ensembl
Outerchr8:42069647..42114305hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3844659
hg1944659
hg1844659
hg1744659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643
SamplesNA12878
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)nsv6168
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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