A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1509



Internal ID15199386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:42579275..42612382hg38UCSC Ensembl
Outerchr15:42871473..42904580hg19UCSC Ensembl
Outerchr15:40658765..40691872hg18UCSC Ensembl
Outerchr15:40658765..40691872hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg386330
hg196330
hg186330
hg176330
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7160
SamplesNA12156
Known GenesSTARD9
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)nsv1509
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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