A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10295



Internal ID15542503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:47802355..47894432hg38UCSC Ensembl
Outerchr20:46431099..46523176hg19UCSC Ensembl
Outerchr20:45864506..45956583hg18UCSC Ensembl
Outerchr20:45864506..45956583hg17UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg3892078
hg1992078
hg1892078
hg1792078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7344
Supporting Variants
SamplesNA18956
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)nssv10295
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