A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4029



Internal ID15548697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:137189119..137226525hg38UCSC Ensembl
Outerchr3:136907961..136945367hg19UCSC Ensembl
Outerchr3:138390651..138428057hg18UCSC Ensembl
Outerchr3:138390659..138428065hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3837407
hg1937407
hg1837407
hg1737407
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7870
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)nsv4029
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