A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10411



Internal ID15195701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:87926143..87975608hg38UCSC Ensembl
Outerchr4:88847295..88896760hg19UCSC Ensembl
Outerchr4:89066319..89115784hg18UCSC Ensembl
Outerchr4:89204474..89253939hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3849466
hg1949466
hg1849466
hg1749466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7364
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)nssv10411
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