A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6090



Internal ID15204279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:15553229..15586844hg38UCSC Ensembl
Outerchr8:15410738..15444353hg19UCSC Ensembl
Outerchr8:15455109..15488724hg18UCSC Ensembl
Outerchr8:15455109..15488724hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg386111
hg196111
hg186111
hg176111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3630
SamplesNA12878
Known GenesTUSC3
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)nsv6090
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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