A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1668



Internal ID15546231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92042114..92092761hg38UCSC Ensembl
Outerchr15:92585344..92635991hg19UCSC Ensembl
Outerchr15:90386348..90436995hg18UCSC Ensembl
Outerchr15:90386348..90436995hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3850648
hg1950648
hg1850648
hg1750648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5575
SamplesNA19129
Known GenesSLCO3A1
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)nsv1668
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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