A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6688



Internal ID15537175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85403011..85419696hg38UCSC Ensembl
Outerchr16:85436617..85453302hg19UCSC Ensembl
Outerchr16:83994118..84010803hg18UCSC Ensembl
Outerchr16:83994118..84010803hg17UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3816686
hg1916686
hg1816686
hg1716686
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1913
Supporting Variants
SamplesNA12156
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)nssv6688
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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