A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6978



Internal ID15190200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:24292055..24374635hg19UCSC Ensembl
Outerchr22:22622055..22704635hg18UCSC Ensembl
Outerchr22:22616609..22699189hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg1982581
hg1882581
hg1782581
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA12156
Known GenesDDT, DDTL, GSTT2, GSTT2B, GSTTP1, LOC391322
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)nssv6978
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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