A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7475



Internal ID15552488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:85524864..85555203hg38UCSC Ensembl
Outerchr10:87284621..87314960hg19UCSC Ensembl
Outerchr10:87274601..87304940hg18UCSC Ensembl
Outerchr10:87274601..87304940hg17UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg389163
hg199163
hg189163
hg179163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10770
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)nsv7475
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