A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3705



Internal ID15548341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13269356..13286712hg38UCSC Ensembl
Outerchr3:13310856..13328212hg19UCSC Ensembl
Outerchr3:13285856..13303212hg18UCSC Ensembl
Outerchr3:13285856..13303212hg17UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg388254
hg198254
hg188254
hg178254
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6994
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)nsv3705
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