A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3013098



Internal ID15562448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104987916..104987916hg38UCSC Ensembl
chr7:104628363..104628363hg19UCSC Ensembl
chr7:104415599..104415599hg18UCSC Ensembl
chr7:104222314..104222314hg17UCSC Ensembl
Cytoband7q22.2
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 Variantsnsv477014
Supporting Variants
SamplesNA12878
Known GenesLINC01004
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)nssv3013098
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer