A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5610



Internal ID15197147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:69189526..69204933hg38UCSC Ensembl
Outerchr16:69223429..69238836hg19UCSC Ensembl
Outerchr16:67780930..67796337hg18UCSC Ensembl
Outerchr16:67780930..67796337hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg387427
hg197427
hg187427
hg177427
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1851
Supporting Variants
SamplesNA19129
Known GenesSNTB2
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)nssv5610
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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