A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6166



Internal ID15551048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:40299185..40350006hg38UCSC Ensembl
Outerchr8:40156704..40207525hg19UCSC Ensembl
Outerchr8:40275861..40326682hg18UCSC Ensembl
Outerchr8:40275861..40326682hg17UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg3850822
hg1950822
hg1850822
hg1750822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6217, nssv5081
SamplesNA12156, NA19129
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)nsv6166
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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