A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1584



Internal ID15546147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68934506..68943973hg38UCSC Ensembl
Outerchr15:69226845..69236312hg19UCSC Ensembl
Outerchr15:67013899..67023366hg18UCSC Ensembl
Outerchr15:67013899..67023366hg17UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg389468
hg199468
hg189468
hg179468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7191
SamplesNA12156
Known GenesMIR548H4, NOX5, SPESP1
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)nsv1584
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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