A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1868



Internal ID15199745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:72768063..72786155hg38UCSC Ensembl
Outerchr16:72801962..72820054hg19UCSC Ensembl
Outerchr16:71359463..71377555hg18UCSC Ensembl
Outerchr16:71359463..71377555hg17UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3818093
hg1918093
hg1818093
hg1718093
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6678
SamplesNA12156
Known GenesZFHX3
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)nsv1868
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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