A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1657



Internal ID15199534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:89287234..89308299hg38UCSC Ensembl
Outerchr15:89830465..89851530hg19UCSC Ensembl
Outerchr15:87631469..87652534hg18UCSC Ensembl
Outerchr15:87631469..87652534hg17UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821066
hg1921066
hg1821066
hg1721066
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7213
SamplesNA12156
Known GenesFANCI
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)nsv1657
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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