A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1841



Internal ID15199718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:67353227..67386776hg38UCSC Ensembl
Outerchr16:67387130..67420679hg19UCSC Ensembl
Outerchr16:65944631..65978180hg18UCSC Ensembl
Outerchr16:65944631..65978180hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg385886
hg195886
hg185886
hg175886
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7262
SamplesNA12156
Known GenesLRRC36
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)nsv1841
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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