A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1926



Internal ID8513471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88626290..88660544hg38UCSC Ensembl
Outerchr16:88692698..88726952hg19UCSC Ensembl
Outerchr16:87220199..87254453hg18UCSC Ensembl
Outerchr16:87220199..87254453hg17UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg385748
hg195748
hg185748
hg175748
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2958
SamplesNA18555
Known GenesCYBA, IL17C, MVD, ZC3H18
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)nsv1926
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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