A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10083



Internal ID15196028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15805795..15837421hg38UCSC Ensembl
Outerchr16:15899652..15931278hg19UCSC Ensembl
Outerchr16:15807153..15838779hg18UCSC Ensembl
Outerchr16:15807153..15838779hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg387873
hg197873
hg187873
hg177873
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1742
Supporting Variants
SamplesNA18956
Known GenesMYH11
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)nssv10083
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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