A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141959



Internal ID19283176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:163836875..163836967hg38UCSC Ensembl
Outerchr2:164693385..164693477hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993469
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141959
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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