A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3016126



Internal ID15561856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:167796997..167796997hg38UCSC Ensembl
chr3:167514785..167514785hg19UCSC Ensembl
chr3:168997479..168997479hg18UCSC Ensembl
chr3:168997487..168997487hg17UCSC Ensembl
Cytoband3q26.1
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 Variantsnsv475706
Supporting Variants
SamplesNA12878
Known GenesSERPINI1
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)nssv3016126
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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