A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3013636



Internal ID15565789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105230014..105230014hg38UCSC Ensembl
chr2:105846471..105846471hg19UCSC Ensembl
chr2:105212903..105212903hg18UCSC Ensembl
chr2:105304989..105304989hg17UCSC Ensembl
Cytoband2q12.1
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 Variantsnsv472738
Supporting Variants
SamplesNA18555
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)nssv3013636
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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