A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv476424



Internal ID15229176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:30537495..30537495hg38UCSC Ensembl
chr19:31028402..31028402hg19UCSC Ensembl
chr19:35720242..35720242hg18UCSC Ensembl
chr19:35720242..35720242hg17UCSC Ensembl
Cytoband19q12
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 Variantsnssv3020016
SamplesNA12878
Known GenesZNF536
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)nsv476424
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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