A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1802



Internal ID15546365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:49339758..49371879hg38UCSC Ensembl
Outerchr16:49373669..49405790hg19UCSC Ensembl
Outerchr16:47931170..47963291hg18UCSC Ensembl
Outerchr16:47931170..47963291hg17UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg387159
hg197159
hg187159
hg177159
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5603
SamplesNA19129
Known Genes
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)nsv1802
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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