A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1659



Internal ID15545407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:17472833..17520531hg38UCSC Ensembl
Outerchr3:17514325..17562023hg19UCSC Ensembl
Outerchr3:17489329..17537027hg18UCSC Ensembl
Outerchr3:17489329..17537027hg17UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3847699
hg1947699
hg1847699
hg1747699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3715
Supporting Variants
SamplesNA19240
Known GenesTBC1D5
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)nssv1659
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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