A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1007027



Internal ID6719142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:103958468..104083991hg38UCSC Ensembl
OuterchrX:103213041..103328676hg19UCSC Ensembl
OuterchrX:103099697..103215332hg18UCSC Ensembl
CytobandXq22.2
Allele length
AssemblyAllele length
hg38125524
hg19115636
hg18115636
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3564812
SamplesHuRef
Known GenesH2BFM, H2BFWT, H2BFXP, MIR1256, TMSB15B
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv1007027
Frequency
Sample Size3
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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