A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5926



Internal ID15196765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:23929223..23972420hg38UCSC Ensembl
Outerchr22:24271410..24314609hg19UCSC Ensembl
Outerchr22:22601410..22644609hg18UCSC Ensembl
Outerchr22:22595964..22639163hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3843198
hg1943200
hg1843200
hg1743200
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA19129
Known GenesDDT, DDTL, GSTT2, GSTT2B
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)nssv5926
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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