A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5954



Internal ID15204129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:17277953..17320853hg38UCSC Ensembl
Outerchr10:17319952..17362852hg19UCSC Ensembl
Outerchr10:17359958..17402858hg18UCSC Ensembl
Outerchr10:17359958..17402858hg17UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3842901
hg1942901
hg1842901
hg1742901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8462
SamplesNA12156
Known GenesST8SIA6
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)nsv5954
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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