A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3390



Internal ID15201309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:44640957..44707899hg38UCSC Ensembl
Outerchr20:43269598..43336540hg19UCSC Ensembl
Outerchr20:42703012..42769954hg18UCSC Ensembl
Outerchr20:42703012..42769954hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3866943
hg1966943
hg1866943
hg1766943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1604, nssv7684
SamplesNA12156, NA19240
Known GenesADA, LOC79015
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)nsv3390
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