A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1892



Internal ID15546455
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 StatusM
Merged Variants
Supporting Variantsnssv5616, nssv6686
SamplesNA12156, NA19129
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)nsv1892
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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