A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3745



Internal ID15548385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:28142428..28157500hg38UCSC Ensembl
Outerchr3:28183919..28198991hg19UCSC Ensembl
Outerchr3:28158923..28173995hg18UCSC Ensembl
Outerchr3:28158923..28173995hg17UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3815073
hg1915073
hg1815073
hg1715073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv11057
SamplesNA15510
Known Genes
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)nsv3745
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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