A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1834



Internal ID15546397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:65855415..65857180hg38UCSC Ensembl
Outerchr16:65889318..65891083hg19UCSC Ensembl
Outerchr16:64446819..64448584hg18UCSC Ensembl
Outerchr16:64446819..64448584hg17UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387542
hg197542
hg187542
hg177542
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1310
SamplesNA19240
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)nsv1834
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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