A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9606



Internal ID15193022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:21398843..21571877hg38UCSC Ensembl
Outerchr22:21753132..21926166hg19UCSC Ensembl
Outerchr22:20083132..20256166hg18UCSC Ensembl
Outerchr22:20077686..20250720hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38173035
hg19173035
hg18173035
hg17173035
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA18507
Known GenesHIC2, PI4KAP2, RIMBP3B, RIMBP3C, TMEM191C, UBE2L3
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)nssv9606
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