A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483



Internal ID15204711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:14701615..14731881hg38UCSC Ensembl
Outerchr9:14701613..14731879hg19UCSC Ensembl
Outerchr9:14691613..14721879hg18UCSC Ensembl
Outerchr9:14691613..14721879hg17UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg389013
hg199013
hg189013
hg179013
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5150
SamplesNA19129
Known GenesCER1
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)nsv6483
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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