A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv480725



Internal ID15233465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26132126..26132126hg38UCSC Ensembl
chr16:26143447..26143447hg19UCSC Ensembl
chr16:26050948..26050948hg18UCSC Ensembl
chr16:26050948..26050948hg17UCSC Ensembl
Cytoband16p12.1
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 Variantsnssv3017424
Samples
Known GenesHS3ST4
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)nsv480725
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