A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5749084



Internal ID9440251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:82537567..82546323hg38UCSC Ensembl
OuterchrX:82537196..82546693hg38UCSC Ensembl
InnerchrX:81793016..81801772hg19UCSC Ensembl
OuterchrX:81792645..81802142hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg389498
hg199498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675944
Supporting Variants
SamplesNA18638
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5749084
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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