A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1533992



Internal ID12697113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:50887920..50895981hg38UCSC Ensembl
chr3:50925351..50934970hg19UCSC Ensembl
chr3:50900409..50910036hg18UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg388062
hg199620
hg189628
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3727871
SamplesHuRef
Known GenesDOCK3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1533992
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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