A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3018466



Internal ID15215901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38981694..38981694hg38UCSC Ensembl
chr7:39021294..39021294hg19UCSC Ensembl
chr7:38987819..38987819hg18UCSC Ensembl
chr7:38794534..38794534hg17UCSC Ensembl
Cytoband7p14.1
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 Variantsnsv476114
Supporting Variants
SamplesNA12878
Known GenesPOU6F2
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)nssv3018466
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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