A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1286



Internal ID15197750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:841712..848088hg38UCSC Ensembl
Outerchr16:891712..898088hg19UCSC Ensembl
Outerchr16:831713..838089hg18UCSC Ensembl
Outerchr16:831713..838089hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389875
hg199875
hg189875
hg179875
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1704
Supporting Variants
SamplesNA19240
Known Genes
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)nssv1286
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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