A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120122



Internal ID18916569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:33539511..33542809hg38UCSC Ensembl
Outerchr2:33764578..33767876hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg383299
hg193299
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960876
SamplesKWS1
Known GenesRASGRP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120122
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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