A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3779



Internal ID15201736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:41292209..41809712hg38UCSC Ensembl
Outerchr3:41333700..41851204hg19UCSC Ensembl
Outerchr3:41308704..41826208hg18UCSC Ensembl
Outerchr3:41308704..41826208hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38517504
hg19517505
hg18517505
hg17517505
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1670, nssv7794
SamplesNA12156, NA19240
Known GenesULK4
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)nsv3779
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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