A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5433



Internal ID15550242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:108642290..108670946hg38UCSC Ensembl
Outerchr6:108963493..108992149hg19UCSC Ensembl
Outerchr6:109070186..109098842hg18UCSC Ensembl
Outerchr6:109070186..109098842hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387169
hg197169
hg187169
hg177169
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2611
SamplesNA18555
Known GenesFOXO3
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)nsv5433
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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