A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4141



Internal ID15548821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:180072102..180105190hg38UCSC Ensembl
Outerchr3:179789890..179822978hg19UCSC Ensembl
Outerchr3:181272584..181305672hg18UCSC Ensembl
Outerchr3:181272592..181305680hg17UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg386350
hg196350
hg186350
hg176350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7900
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)nsv4141
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer