A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7339



Internal ID15552338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:11064977..12979471hg38UCSC Ensembl
Outerchr20:11045625..12960119hg19UCSC Ensembl
Outerchr20:10993625..12908119hg18UCSC Ensembl
Outerchr20:10993625..12908119hg17UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg381914495
hg191914495
hg181914495
hg171914495
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9364
SamplesNA18517
Known GenesBTBD3, LOC339593
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)nsv7339
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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