A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9764



Internal ID15540086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42638806..42688034hg38UCSC Ensembl
Outerchr9:44283085..44332313hg19UCSC Ensembl
Outerchr9:44223081..44272309hg18UCSC Ensembl
Outerchr9:43434158..43483386hg17UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3849229
hg1949229
hg1849229
hg1749229
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7423
Supporting Variants
SamplesNA18507
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)nssv9764
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