A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565204



Internal ID7036586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:233562682..233577886hg38UCSC Ensembl
Outerchr2:234471328..234486532hg19UCSC Ensembl
Outerchr2:234135025..234154379hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3815205
hg1915205
hg1819355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv992038
Supporting Variants
SamplesHuRef
Known GenesUSP40
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565204
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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