A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4159804



Internal ID11442342
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 StatusS
Merged Variantsesv1226673
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4159804
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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