A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv476473



Internal ID15229225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:61346356..61346356hg38UCSC Ensembl
chr18:59013589..59013589hg19UCSC Ensembl
chr18:57164569..57164569hg18UCSC Ensembl
chr18:57164569..57164569hg17UCSC Ensembl
Cytoband18q21.33
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 Variantsnssv3015226
SamplesNA12878
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)nsv476473
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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