A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3018686



Internal ID15222410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:153052432..153052432hg38UCSC Ensembl
chrX:152220791..152220791hg19UCSC Ensembl
chrX:151971447..151971447hg18UCSC Ensembl
chrX:151891360..151891360hg17UCSC Ensembl
CytobandXq28
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 Variantsnsv480500
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)nssv3018686
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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