A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3012113



Internal ID15569037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28397973..28397973hg38UCSC Ensembl
chr1:28724484..28724484hg19UCSC Ensembl
chr1:28597071..28597071hg18UCSC Ensembl
chr1:28408626..28408626hg17UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv479595
Supporting Variants
Samples
Known GenesPHACTR4
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)nssv3012113
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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