A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9514



Internal ID15539800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:47171642..47189767hg38UCSC Ensembl
Outerchr15:47463839..47481964hg19UCSC Ensembl
Outerchr15:45251131..45269256hg18UCSC Ensembl
Outerchr15:45251131..45269256hg17UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg3818568
hg1918568
hg1818568
hg1718568
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1525
Supporting Variants
SamplesNA18507
Known GenesSEMA6D
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)nssv9514
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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