A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3941



Internal ID15548601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:110666943..110711676hg38UCSC Ensembl
Outerchr3:110385790..110430523hg19UCSC Ensembl
Outerchr3:111868480..111913213hg18UCSC Ensembl
Outerchr3:111868480..111913213hg17UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3844734
hg1944734
hg1844734
hg1744734
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7846
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)nsv3941
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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