A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11205



Internal ID15192688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:123978917..124029482hg38UCSC Ensembl
Outerchr9:126741196..126791761hg19UCSC Ensembl
Outerchr9:125781017..125831582hg18UCSC Ensembl
Outerchr9:123820750..123871315hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3850566
hg1950566
hg1850566
hg1750566
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7435
Supporting Variants
SamplesNA15510
Known GenesLHX2
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)nssv11205
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