A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3017042



Internal ID15218538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184644764..184644764hg38UCSC Ensembl
chr4:185565918..185565918hg19UCSC Ensembl
chr4:185802912..185802912hg18UCSC Ensembl
chr4:185941067..185941067hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv477526
Supporting Variants
SamplesNA18517
Known GenesCASP3
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)nssv3017042
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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