A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1851



Internal ID15199728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:69162460..69204933hg38UCSC Ensembl
Outerchr16:69196363..69238836hg19UCSC Ensembl
Outerchr16:67753864..67796337hg18UCSC Ensembl
Outerchr16:67753864..67796337hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385822
hg195822
hg185822
hg175822
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4222, nssv7267, nssv2147, nssv5610
SamplesNA12156, NA12878, NA18555, NA19129
Known GenesCIRH1A, SNTB2
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)nsv1851
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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