A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007512



Internal ID7072607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:19603735..19620316hg38UCSC Ensembl
Outerchr1:19930229..19946810hg19UCSC Ensembl
Outerchr1:19802816..19819397hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3816582
hg1916582
hg1816582
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3565353
SamplesHuRef
Known GenesMINOS1, MINOS1-NBL1, RPS14P3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007512
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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