A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1734793



Internal ID5864893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691432..3691487hg38UCSC Ensembl
chrX:3609473..3609528hg19UCSC Ensembl
chrX:3619473..3619528hg18UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3856
hg1956
hg1856
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4227239
SamplesHuRef
Known GenesPRKX
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1734793
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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