A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3011999



Internal ID15563225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80793410..80793410hg38UCSC Ensembl
chr7:80422726..80422726hg19UCSC Ensembl
chr7:80260662..80260662hg18UCSC Ensembl
chr7:80067377..80067377hg17UCSC Ensembl
Cytoband7q21.11
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 Variantsnsv474274
Supporting Variants
SamplesNA18507
Known GenesSEMA3C
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)nssv3011999
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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