A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7503



Internal ID15205833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:96648365..96678896hg38UCSC Ensembl
Outerchr10:98408122..98438653hg19UCSC Ensembl
Outerchr10:98398112..98428643hg18UCSC Ensembl
Outerchr10:98398112..98428643hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg388738
hg198738
hg188738
hg178738
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5306
SamplesNA19129
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)nsv7503
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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