A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960876



Internal ID18877749
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 StatusS
Merged Variantsnsv1120122
Supporting Variants
SamplesKWS1
Known GenesRASGRP3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960876
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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