A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3798



Internal ID15201757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:46737140..46824116hg38UCSC Ensembl
Outerchr3:46778630..46865606hg19UCSC Ensembl
Outerchr3:46753634..46840610hg18UCSC Ensembl
Outerchr3:46753634..46840610hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3886977
hg1986977
hg1886977
hg1786977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9617, nssv1674, nssv5961
SamplesNA18507, NA19240, NA19129
Known GenesPRSS45
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)nsv3798
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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