A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6686



Internal ID15551620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:116069287..116100768hg38UCSC Ensembl
Outerchr9:118831566..118863047hg19UCSC Ensembl
Outerchr9:117871387..117902868hg18UCSC Ensembl
Outerchr9:115911120..115942601hg17UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg388264
hg198264
hg188264
hg178264
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745
SamplesNA12878
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)nsv6686
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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