A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv475434



Internal ID15228186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:24165711..24165711hg38UCSC Ensembl
chr12:24318645..24318645hg19UCSC Ensembl
chr12:24209912..24209912hg18UCSC Ensembl
chr12:24209912..24209912hg17UCSC Ensembl
Cytoband12p12.1
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 Variantsnssv3020023
SamplesNA19240
Known GenesSOX5
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)nsv475434
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer