A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1226673



Internal ID12389796
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:154395056..154398179hg38UCSC Ensembl
chrX:153623398..153626520hg19UCSC Ensembl
chrX:153276592..153279714hg18UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg383124
hg193123
hg183123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4159804
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1226673
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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