A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1003988



Internal ID6716114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:20618088..20700191hg38UCSC Ensembl
Outerchr19:20800894..20882997hg19UCSC Ensembl
Outerchr19:20592734..20674837hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3882104
hg1982104
hg1882104
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565221
SamplesHuRef
Known GenesZNF626
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1003988
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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