A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5585



Internal ID15197177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3695766..3723046hg38UCSC Ensembl
Outerchr16:3745767..3773047hg19UCSC Ensembl
Outerchr16:3685768..3713048hg18UCSC Ensembl
Outerchr16:3685768..3713048hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3811996
hg1911996
hg1811996
hg1711996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1717
Supporting Variants
SamplesNA19129
Known GenesTRAP1
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)nssv5585
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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