A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1771



Internal ID15546334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:26146892..26198022hg38UCSC Ensembl
Outerchr16:26158213..26209343hg19UCSC Ensembl
Outerchr16:26065714..26116844hg18UCSC Ensembl
Outerchr16:26065714..26116844hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386377
hg196377
hg186377
hg176377
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7241, nssv1302, nssv5599, nssv4206
SamplesNA12156, NA12878, NA19240, NA19129
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)nsv1771
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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