A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4090



Internal ID15202079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:161136946..161169046hg38UCSC Ensembl
Outerchr3:160854734..160886834hg19UCSC Ensembl
Outerchr3:162337428..162369528hg18UCSC Ensembl
Outerchr3:162337436..162369536hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg388753
hg198753
hg188753
hg178753
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7045, nssv345
SamplesNA12156, NA19240
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)nsv4090
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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