A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3565676



Internal ID7037058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:91438775..91453364hg38UCSC Ensembl
Outerchr10:93198532..93213121hg19UCSC Ensembl
Outerchr10:93188512..93203101hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3814590
hg1914590
hg1814590
Variant TypeOTHER inversion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1003018
Supporting Variants
SamplesHuRef
Known GenesHECTD2, LOC100188947
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3565676
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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