A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1000442



Internal ID6712586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:66241034..66261067hg38UCSC Ensembl
Outerchr11:66008505..66028538hg19UCSC Ensembl
Outerchr11:65765081..65785114hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3820034
hg1920034
hg1820034
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564035
SamplesHuRef
Known GenesKLC2, PACS1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1000442
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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