A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1773



Internal ID15199650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:27412897..27430529hg38UCSC Ensembl
Outerchr16:27424218..27441850hg19UCSC Ensembl
Outerchr16:27331719..27349351hg18UCSC Ensembl
Outerchr16:27331719..27349351hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg386053
hg196053
hg186053
hg176053
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5600
SamplesNA19129
Known GenesIL21R
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)nsv1773
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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