A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3019972



Internal ID15219244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86960007..86960007hg38UCSC Ensembl
chr9:89574922..89574922hg19UCSC Ensembl
chr9:88764742..88764742hg18UCSC Ensembl
chr9:86804476..86804476hg17UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv471887
Supporting Variants
SamplesNA18555
Known GenesLOC100506834
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nssv3019972
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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