A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2958



Internal ID15194907
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 StatusS
Merged Variantsnsv1926
Supporting Variants
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)nssv2958
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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