A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7299



Internal ID15552294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:77746490..77785153hg38UCSC Ensembl
Outerchr10:79506248..79544911hg19UCSC Ensembl
Outerchr10:79176254..79214917hg18UCSC Ensembl
Outerchr10:79176254..79214917hg17UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385632
hg195632
hg185632
hg175632
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8819, nssv10766
SamplesNA12156, NA18956
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv7299
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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