A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6146



Internal ID15551026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:33505413..33550725hg38UCSC Ensembl
Outerchr8:33362931..33408243hg19UCSC Ensembl
Outerchr8:33482473..33527785hg18UCSC Ensembl
Outerchr8:33482473..33527785hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3845313
hg1945313
hg1845313
hg1745313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8480
SamplesNA12156
Known GenesRNF122, TTI2
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)nsv6146
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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