A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5560



Internal ID15543892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66099710..66104391hg38UCSC Ensembl
Outerchr15:66392048..66396729hg19UCSC Ensembl
Outerchr15:64179102..64183783hg18UCSC Ensembl
Outerchr15:64179102..64183783hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812177
hg1912177
hg1812177
hg1712177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1573
Supporting Variants
SamplesNA19129
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)nssv5560
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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