A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4703



Internal ID15542998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187421486..187461545hg38UCSC Ensembl
Outerchr3:187139274..187179333hg19UCSC Ensembl
Outerchr3:188621968..188662027hg18UCSC Ensembl
Outerchr3:188621976..188662035hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3840060
hg1940060
hg1840060
hg1740060
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7357
Supporting Variants
SamplesNA19129
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)nssv4703
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