A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6968



Internal ID15190210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:21437459..21459316hg38UCSC Ensembl
Outerchr22:21791748..21813605hg19UCSC Ensembl
Outerchr22:20121748..20143605hg18UCSC Ensembl
Outerchr22:20116302..20138159hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3821858
hg1921858
hg1821858
hg1721858
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7350
Supporting Variants
SamplesNA12156
Known GenesHIC2
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)nssv6968
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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