A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1141989



Internal ID19265209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:94578132..94593318hg38UCSC Ensembl
Outerchr4:95499283..95514469hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg3815187
hg1915187
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3993501
SamplesKWS2
Known GenesPDLIM5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1141989
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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