A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5921559



Internal ID8898962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:75806128..75922895hg38UCSC Ensembl
chrX:75025963..75142730hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38116768
hg19116768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672416
Supporting Variants
SamplesHG01069
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5921559
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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