A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10786



Internal ID15542012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:126627441..126630240hg38UCSC Ensembl
Outerchr10:128316010..128318809hg19UCSC Ensembl
Outerchr10:128306000..128308799hg18UCSC Ensembl
Outerchr10:128306000..128308799hg17UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg386746
hg196746
hg186746
hg176746
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7603
Supporting Variants
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)nssv10786
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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