A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1482



Internal ID15199359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:32790965..32821443hg38UCSC Ensembl
Outerchr15:33083166..33113644hg19UCSC Ensembl
Outerchr15:30870458..30900936hg18UCSC Ensembl
Outerchr15:30870458..30900936hg17UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3830479
hg1930479
hg1830479
hg1730479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7155
SamplesNA12156
Known GenesFMN1
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)nsv1482
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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