A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565672



Internal ID6690368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr21:10342055..10530741hg38UCSC Ensembl
Outerchr21:10981716..11170402hg19UCSC Ensembl
Outerchr21:10003587..10192273hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38188687
hg19188687
hg18188687
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv991443
Supporting Variants
SamplesHuRef
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565672
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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