A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1513



Internal ID15199390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43362170..43396516hg38UCSC Ensembl
Outerchr15:43654368..43688714hg19UCSC Ensembl
Outerchr15:41441660..41476006hg18UCSC Ensembl
Outerchr15:41441660..41476006hg17UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg385680
hg195680
hg185680
hg175680
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2931
SamplesNA18555
Known GenesRNU6-28P, TUBGCP4, ZSCAN29
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)nsv1513
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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