A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3771



Internal ID15548414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:39015820..39042832hg38UCSC Ensembl
Outerchr3:39057311..39084323hg19UCSC Ensembl
Outerchr3:39032315..39059327hg18UCSC Ensembl
Outerchr3:39032315..39059327hg17UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg386094
hg196094
hg186094
hg176094
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5958
SamplesNA19129
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)nsv3771
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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