A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6152



Internal ID15204347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:35678315..35711831hg38UCSC Ensembl
Outerchr8:35535833..35569349hg19UCSC Ensembl
Outerchr8:35655375..35688891hg18UCSC Ensembl
Outerchr8:35655375..35688891hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg385771
hg195771
hg185771
hg175771
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5075
SamplesNA19129
Known GenesUNC5D
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)nsv6152
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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