A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1719



Internal ID15546282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4094898..4139626hg38UCSC Ensembl
Outerchr16:4144899..4189627hg19UCSC Ensembl
Outerchr16:4084900..4129628hg18UCSC Ensembl
Outerchr16:4084900..4129628hg17UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3844729
hg1944729
hg1844729
hg1744729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7226
SamplesNA12156
Known GenesADCY9
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)nsv1719
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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