A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078



Internal ID15550951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:10290248..10325421hg38UCSC Ensembl
Outerchr8:10147758..10182931hg19UCSC Ensembl
Outerchr8:10185168..10220341hg18UCSC Ensembl
Outerchr8:10185168..10220341hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg384572
hg194572
hg184572
hg174572
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626
SamplesNA12878
Known GenesMSRA
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)nsv6078
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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