A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6667



Internal ID15204913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:111781113..111810228hg38UCSC Ensembl
Outerchr9:114543393..114572508hg19UCSC Ensembl
Outerchr9:113583214..113612329hg18UCSC Ensembl
Outerchr9:111622948..111652063hg17UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385923
hg195923
hg185923
hg175923
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824
SamplesNA19240
Known GenesC9orf84
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)nsv6667
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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