A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960889



Internal ID19208576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:42755710..42759572hg38UCSC Ensembl
Outerchr22:43151716..43155578hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg383863
hg193863
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120134
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960889
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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