A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129335



Internal ID18924372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:36201824..36255456hg38UCSC Ensembl
Outerchr22:36597870..36651502hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3853633
hg1953633
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962768
SamplesKWS1
Known GenesAPOL1, APOL2, APOL4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129335
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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