A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5403152



Internal ID9186139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:81805917..81811823hg38UCSC Ensembl
OuterchrX:81805396..81812493hg38UCSC Ensembl
InnerchrX:81061416..81067322hg19UCSC Ensembl
OuterchrX:81060895..81067992hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg387098
hg197098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664457
Supporting Variants
SamplesHG01456
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5403152
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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