A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6967



Internal ID15190211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:21404274..21571213hg38UCSC Ensembl
Outerchr22:21758563..21925502hg19UCSC Ensembl
Outerchr22:20088563..20255502hg18UCSC Ensembl
Outerchr22:20083117..20250056hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38166940
hg19166940
hg18166940
hg17166940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA12156
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)nssv6967
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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