A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv480027



Internal ID15232767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153051791..153051791hg38UCSC Ensembl
chrX:152220150..152220150hg19UCSC Ensembl
chrX:151970806..151970806hg18UCSC Ensembl
chrX:151890719..151890719hg17UCSC Ensembl
CytobandXq28
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 Variantsnssv3018478
Samples
Known Genes
MethodSequencing
Analysis
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA contig. The coordinate provided is from the mappable end of a contig assembled from multiple read pairs, and indicates the genomic vicinity of a novel sequence insertion.
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv480027
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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