A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv474864



Internal ID15574296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:9144733..9144733hg38UCSC Ensembl
chrX:9112774..9112774hg19UCSC Ensembl
chrX:9072774..9072774hg18UCSC Ensembl
chrX:8922510..8922510hg17UCSC Ensembl
CytobandXp22.31
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 Variantsnssv3018361
SamplesNA18956
Known Genes
MethodSequencing
AnalysisSearch fosmid ESPs as described in Tuzun et al (2005)
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA singleton. The coordinate provided is from the mappable member of a fosmid end sequence pair, and indicates the genomic vicinity of a novel sequence insertion
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv474864
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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