A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928



Internal ID15548586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:103822498..103867523hg38UCSC Ensembl
Outerchr3:103541342..103586367hg19UCSC Ensembl
Outerchr3:105024032..105069057hg18UCSC Ensembl
Outerchr3:105024032..105069057hg17UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3845026
hg1945026
hg1845026
hg1745026
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7840
SamplesNA12156
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)nsv3928
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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