A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5922



Internal ID15196769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:21404562..21491445hg38UCSC Ensembl
Outerchr22:21758851..21845734hg19UCSC Ensembl
Outerchr22:20088851..20175734hg18UCSC Ensembl
Outerchr22:20083405..20170288hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3886884
hg1986884
hg1886884
hg1786884
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA19129
Known GenesHIC2, PI4KAP2, TMEM191C
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)nssv5922
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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