A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6511289



Internal ID9788657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:819814..867357hg38UCSC Ensembl
chrX:780549..828092hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3847544
hg1947544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2661336
Supporting Variants
SamplesNA19780
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6511289
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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