A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1745



Internal ID15199622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15974908..15980688hg38UCSC Ensembl
Outerchr16:16068765..16074545hg19UCSC Ensembl
Outerchr16:15976266..15982046hg18UCSC Ensembl
Outerchr16:15976266..15982046hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3820141
hg1920141
hg1820141
hg1720141
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9524
SamplesNA18507
Known GenesABCC1
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)nsv1745
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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