A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5876055



Internal ID9387428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135398286..135401512hg38UCSC Ensembl
OuterchrX:135398129..135401665hg38UCSC Ensembl
InnerchrX:134532211..134535437hg19UCSC Ensembl
OuterchrX:134532054..134535590hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg383537
hg193537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661672
Supporting Variants
SamplesNA18582
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5876055
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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