A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv473721



Internal ID15573153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168147246..168147246hg38UCSC Ensembl
chr5:167574251..167574251hg19UCSC Ensembl
chr5:167506829..167506829hg18UCSC Ensembl
chr5:167506829..167506829hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3018619
SamplesNA19129
Known GenesTENM2
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)nsv473721
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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