A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7594



Internal ID15552619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125233189..125262129hg38UCSC Ensembl
Outerchr10:126921758..126950698hg19UCSC Ensembl
Outerchr10:126911748..126940688hg18UCSC Ensembl
Outerchr10:126911748..126940688hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3810564
hg1910564
hg1810564
hg1710564
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10784
SamplesNA18956
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)nsv7594
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