A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4036



Internal ID15548705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:140012918..140020002hg38UCSC Ensembl
Outerchr3:139731760..139738844hg19UCSC Ensembl
Outerchr3:141214450..141221534hg18UCSC Ensembl
Outerchr3:141214458..141221542hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg385620
hg195620
hg185620
hg175620
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7873
SamplesNA12156
Known GenesCLSTN2
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)nsv4036
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