A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7264



Internal ID15536600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:68054336..68070901hg38UCSC Ensembl
Outerchr16:68088239..68104804hg19UCSC Ensembl
Outerchr16:66645740..66662305hg18UCSC Ensembl
Outerchr16:66645740..66662305hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3816566
hg1916566
hg1816566
hg1716566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1845
Supporting Variants
SamplesNA12156
Known GenesDUS2
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)nssv7264
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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