A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2110



Internal ID15541393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66093065..66103364hg38UCSC Ensembl
Outerchr15:66385403..66395702hg19UCSC Ensembl
Outerchr15:64172457..64182756hg18UCSC Ensembl
Outerchr15:64172457..64182756hg17UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812337
hg1912337
hg1812337
hg1712337
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1573
Supporting Variants
SamplesNA18555
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)nssv2110
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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