A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5616



Internal ID15543825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:79067719..79080860hg38UCSC Ensembl
Outerchr16:79101616..79114757hg19UCSC Ensembl
Outerchr16:77659117..77672258hg18UCSC Ensembl
Outerchr16:77659117..77672258hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3813142
hg1913142
hg1813142
hg1713142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1892
Supporting Variants
SamplesNA19129
Known GenesWWOX
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)nssv5616
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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