A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479529



Internal ID15578955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50379053..50379053hg38UCSC Ensembl
chr7:50446751..50446751hg19UCSC Ensembl
chr7:50414245..50414245hg18UCSC Ensembl
chr7:50220960..50220960hg17UCSC Ensembl
Cytoband7p12.2
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 Variantsnssv3013803
Samples
Known GenesIKZF1
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)nsv479529
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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