A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7617



Internal ID15205958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:129504222..129537779hg38UCSC Ensembl
Outerchr10:131302486..131336043hg19UCSC Ensembl
Outerchr10:131192476..131226033hg18UCSC Ensembl
Outerchr10:131192476..131226033hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385716
hg195716
hg185716
hg175716
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5329
SamplesNA19129
Known GenesMGMT
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)nsv7617
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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