A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3758



Internal ID15201713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:33818194..33852645hg38UCSC Ensembl
Outerchr3:33859686..33894137hg19UCSC Ensembl
Outerchr3:33834690..33869141hg18UCSC Ensembl
Outerchr3:33834690..33869141hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385576
hg195576
hg185576
hg175576
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3091
SamplesNA18555
Known GenesPDCD6IP
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)nsv3758
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