A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9617



Internal ID15193011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:46737140..46819625hg38UCSC Ensembl
Outerchr3:46778630..46861115hg19UCSC Ensembl
Outerchr3:46753634..46836119hg18UCSC Ensembl
Outerchr3:46753634..46836119hg17UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3882486
hg1982486
hg1882486
hg1782486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3798
Supporting Variants
SamplesNA18507
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)nssv9617
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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