A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6686



Internal ID15537177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:79035381..79080865hg38UCSC Ensembl
Outerchr16:79069278..79114762hg19UCSC Ensembl
Outerchr16:77626779..77672263hg18UCSC Ensembl
Outerchr16:77626779..77672263hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3845485
hg1945485
hg1845485
hg1745485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1892
Supporting Variants
SamplesNA12156
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)nssv6686
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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