A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10932



Internal ID15539520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66098753..66104116hg38UCSC Ensembl
Outerchr15:66391091..66396454hg19UCSC Ensembl
Outerchr15:64178145..64183508hg18UCSC Ensembl
Outerchr15:64178145..64183508hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3811047
hg1911047
hg1811047
hg1711047
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1573
Supporting Variants
SamplesNA15510
Known GenesMEGF11
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)nssv10932
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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