A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3366



Internal ID15547968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:35828492..35852758hg38UCSC Ensembl
Outerchr20:34416414..34440680hg19UCSC Ensembl
Outerchr20:33879828..33904094hg18UCSC Ensembl
Outerchr20:33879828..33904094hg17UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3812424
hg1912424
hg1812424
hg1712424
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9598
SamplesNA18507
Known GenesPHF20
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)nsv3366
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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