A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3016837



Internal ID15216636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91802714..91802714hg38UCSC Ensembl
chr1:92268271..92268271hg19UCSC Ensembl
chr1:92040859..92040859hg18UCSC Ensembl
chr1:91980292..91980292hg17UCSC Ensembl
Cytoband1p22.1
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 Variantsnsv478843
Supporting Variants
SamplesNA18507
Known GenesTGFBR3
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)nssv3016837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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