A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv479819



Internal ID15232559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:148362066..148362066hg38UCSC Ensembl
chr7:148059158..148059158hg19UCSC Ensembl
chr7:147690091..147690091hg18UCSC Ensembl
chr7:147496806..147496806hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg381
hg191
hg181
hg171
Variant TypeCNV novel sequence insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3014901
Samples
Known GenesCNTNAP2
MethodSequencing
Analysis
PlatformAgilent Custom Human 244K CGH Array
CommentsOEA contig. The coordinate provided is from the mappable end of a contig assembled from multiple read pairs, and indicates the genomic vicinity of a novel sequence insertion.
ReferenceKidd_et_al_2010
Pubmed ID20440878
Accession Number(s)nsv479819
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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