A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv481162



Internal ID15580588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1572860..1572860hg38UCSC Ensembl
chr11:1594090..1594090hg19UCSC Ensembl
chr11:1550666..1550666hg18UCSC Ensembl
chr11:1550666..1550666hg17UCSC Ensembl
Cytoband11p15.5
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 Variantsnssv3013272
Samples
Known GenesKRTAP5-AS1, MOB2
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)nsv481162
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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