A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6345606



Internal ID9020405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:138282583..138283032hg38UCSC Ensembl
chrX:137364742..137365191hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664537
Supporting Variants
SamplesHG00638
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6345606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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