A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3750



Internal ID15548391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32055081..32075260hg38UCSC Ensembl
Outerchr3:32096573..32116752hg19UCSC Ensembl
Outerchr3:32071577..32091756hg18UCSC Ensembl
Outerchr3:32071577..32091756hg17UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3820180
hg1920180
hg1820180
hg1720180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3155, nssv2392
SamplesNA12878, NA18555
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)nsv3750
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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