A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479038



Internal ID15578464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:119269064..119269064hg38UCSC Ensembl
chrX:118403027..118403027hg19UCSC Ensembl
chrX:118287055..118287055hg18UCSC Ensembl
chrX:118184909..118184909hg17UCSC Ensembl
CytobandXq24
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 Variantsnssv3012181
Samples
Known Genes
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)nsv479038
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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