A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9433



Internal ID15193698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:248473976..248654587hg38UCSC Ensembl
Outerchr1:248637277..248817888hg19UCSC Ensembl
Outerchr1:246703900..246884511hg18UCSC Ensembl
Outerchr1:244963318..245143929hg17UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38180612
hg19180612
hg18180612
hg17180612
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7193
Supporting Variants
SamplesNA18517
Known GenesOR2G6, OR2T10, OR2T11, OR2T27, OR2T29, OR2T3, OR2T34, OR2T35, OR2T5
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)nssv9433
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