A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3849



Internal ID15201813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:63632791..63666859hg38UCSC Ensembl
Outerchr3:63618467..63652535hg19UCSC Ensembl
Outerchr3:63593507..63627575hg18UCSC Ensembl
Outerchr3:63593507..63627575hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg385369
hg195369
hg185369
hg175369
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7815
SamplesNA12156
Known GenesSNTN
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)nsv3849
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