A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1746874



Internal ID12909992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47233768..47233821hg38UCSC Ensembl
chrX:47093167..47093220hg19UCSC Ensembl
chrX:46978111..46978164hg18UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4135548
SamplesHuRef
Known GenesUSP11
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1746874
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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