A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1735



Internal ID15546298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:11893106..11937740hg38UCSC Ensembl
Outerchr16:11986963..12031597hg19UCSC Ensembl
Outerchr16:11894464..11939098hg18UCSC Ensembl
Outerchr16:11894464..11939098hg17UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3844635
hg1944635
hg1844635
hg1744635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7233
SamplesNA12156
Known GenesGSPT1
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)nsv1735
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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