A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7502



Internal ID15205832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96624946..96669748hg38UCSC Ensembl
Outerchr10:98384703..98429505hg19UCSC Ensembl
Outerchr10:98374693..98419495hg18UCSC Ensembl
Outerchr10:98374693..98419495hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3844803
hg1944803
hg1844803
hg1744803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8831
SamplesNA12156
Known GenesPIK3AP1
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)nsv7502
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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