A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1639



Internal ID15198743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:23913469..23984790hg38UCSC Ensembl
Outerchr22:24255656..24326981hg19UCSC Ensembl
Outerchr22:22585656..22656981hg18UCSC Ensembl
Outerchr22:22580210..22651535hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3871322
hg1971326
hg1871326
hg1771326
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA19240
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)nssv1639
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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