A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145



Internal ID15204339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:33324644..33369268hg38UCSC Ensembl
Outerchr8:33182162..33226786hg19UCSC Ensembl
Outerchr8:33301704..33346328hg18UCSC Ensembl
Outerchr8:33301704..33346328hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3844625
hg1944625
hg1844625
hg1744625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8479
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)nsv6145
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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