A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1779



Internal ID15546342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:29292817..29337558hg38UCSC Ensembl
Outerchr16:29304138..29348879hg19UCSC Ensembl
Outerchr16:29211639..29256380hg18UCSC Ensembl
Outerchr16:29211639..29256380hg17UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3844742
hg1944742
hg1844742
hg1744742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7242
SamplesNA12156
Known GenesSNX29P2
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)nsv1779
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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