A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4028



Internal ID15548696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:137033206..137058511hg38UCSC Ensembl
Outerchr3:136752048..136777353hg19UCSC Ensembl
Outerchr3:138234738..138260043hg18UCSC Ensembl
Outerchr3:138234746..138260051hg17UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3825306
hg1925306
hg1825306
hg1725306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7038
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)nsv4028
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