A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10058



Internal ID15542739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66100006..66111620hg38UCSC Ensembl
Outerchr15:66392344..66403958hg19UCSC Ensembl
Outerchr15:64179398..64191012hg18UCSC Ensembl
Outerchr15:64179398..64191012hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3813154
hg1913154
hg1813154
hg1713154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1573
Supporting Variants
SamplesNA18956
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)nssv10058
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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