A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3012163



Internal ID15223258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99258536..99258536hg38UCSC Ensembl
chr7:98856159..98856159hg19UCSC Ensembl
chr7:98694095..98694095hg18UCSC Ensembl
chr7:98500810..98500810hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv479678
Supporting Variants
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)nssv3012163
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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