A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129409



Internal ID19254349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:27920530..27920606hg38UCSC Ensembl
Outerchr22:28316518..28316594hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962851
SamplesKWS1
Known GenesMIR3199-1, MIR3199-2, TTC28-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129409
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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